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Trial · NCT04428359

A Comparative Study to Assess Efficacy of Intralesional MMR Vaccine and Intralesional Vitamin D3 in Treatment of Warts

NCT04428359, Not applicable, Completed, B.P. Koirala Institute of Health Sciences; results first posted 2021-04-09

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Comparative Study to Assess Efficacy of Intralesional MMR Vaccine and Intralesional Vitamin D3 in Treatment of Warts. Trials, record NCT04428359. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04428359

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
A Comparative Study to Assess Efficacy of Intralesional MMR Vaccine and Intralesional Vitamin D3 in Treatment of Warts
NCT number
NCT04428359
Status
Completed
Phases
Not applicable
Enrollment
66 participants, actual
Lead sponsor
B.P. Koirala Institute of Health Sciences
Conditions
Verruca Viral
Interventions
Measles-Mumps-Rubella Vaccine, Vit D
First posted
2020-06-11
Last updated
2021-04-09
Results first posted
2021-04-09

Source ClinicalTrials.gov

Registered outcomes9

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryEfficacy of IL MMR and IL Vitamin D3 in Treatment of WartsStarting of treatment to end of three months follow-up after completing treatment
Percentage of patients showing complete response to IL MMR and IL Vitamin D3 Complete response -Complete disappearance of warts including distant ones and skin texture at the site is restored to normal (100%) Excellent response- Reduction in size and number including distant ones and few residual warts still visible (75-99%) Good response- Some reduction in size only including that of distant ones but no decrease in number of warts (50-74%) Poor or no response- No significant change in size and number of warts (0-49%)
SecondaryNumber of Participants in Each Education Level GroupAt the time of enrollmentDistribution of wart patients into different education level like professional degree, graduate, intermediate, high school, middle school, primary school or illiterate
SecondaryNumber of Participants in Each Occupation GroupAt the time of enrollmentNumber of participants with different occupations like professional, semiprofessional, clerical/shop/farm, skilled worker, semiskilled worker, unskilled worker, unemployed
SecondaryDurationAt the time of enrollmentDuration of warts
SecondaryEffect of the Warts on Patient's Life as Assessed by Dermatological Life Quality IndexAt the time of enrollment and at the end of three months follow- up after completion of treatment
Quality of life (QoL) will be measured in wart patients, using the Nepali version of the dermatology life quality index (DLQI) questionnaire before initiation of treatment and at the end of follow up. DLQI contains 10 questions that involves 6 sections: symptoms and feelings, daily activities, leisure, work and school, personal relationships and treatment. Questions 1 and 2 assess symptoms and feelings; 3 and 4, daily activities; 5 and 6, leisure; 7, work and school; 8 and 9, personal relationships and 10, treatment. The DLQI consists of 10 questions. Each question is given 4 options from not at all effect (score 0) to very much effect (score 3). The minimum and maximum possible score, thus, is 0 and 30 respectively. Meaning of DLQI Scores 0-1 = no effect at all on patient's life 2-5 = small effect on patient's life 6-10 = moderate effect on patient's life 11-20 = very large effect on patient's life 21-30 = extremely large effect on patient's life .
OtherNumber of WartsAt the time of enrollmentNumber of warts in patients
OtherSizeAt the time of enrollmentSize range of warts
OtherNumber of Participants With Each Progression TypeAt the time of enrollmentNumber of participants with different progressions of warts like Gradual or rapid or stable or regressing lesions
OtherNumber of Participants Who Had Taken Past TreatmentAt the time of enrollmentFrequency of different types of past treatment taken- either traditional or medical treatments

Outcomes9

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYEfficacy of IL MMR and IL Vitamin D3 in Treatment of WartsStarting of treatment to end of three months follow-up after completing treatmentParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants in Each Education Level GroupAt the time of enrollmentParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants in Each Occupation GroupAt the time of enrollmentParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYDurationAt the time of enrollmentmonthsMEAN
SECONDARYEffect of the Warts on Patient's Life as Assessed by Dermatological Life Quality IndexAt the time of enrollment and at the end of three months follow- up after completion of treatmentParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDNumber of WartsAt the time of enrollmentWartsMEAN
OTHER_PRE_SPECIFIEDSizeAt the time of enrollmentcmMEAN
OTHER_PRE_SPECIFIEDNumber of Participants With Each Progression TypeAt the time of enrollmentParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDNumber of Participants Who Had Taken Past TreatmentAt the time of enrollmentParticipantsCOUNT_OF_PARTICIPANTS

Results by group58

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Efficacy of IL MMR and IL Vitamin D3 in Treatment of WartsMeasles, Mumps, Rubella VaccineComplete response25Participants
Efficacy of IL MMR and IL Vitamin D3 in Treatment of WartsVitamin D3Complete response22Participants
Efficacy of IL MMR and IL Vitamin D3 in Treatment of WartsMeasles, Mumps, Rubella VaccineExcellent response2Participants
Efficacy of IL MMR and IL Vitamin D3 in Treatment of WartsVitamin D3Excellent response6Participants
Efficacy of IL MMR and IL Vitamin D3 in Treatment of WartsMeasles, Mumps, Rubella VaccineGood response3Participants
Efficacy of IL MMR and IL Vitamin D3 in Treatment of WartsVitamin D3Good response1Participants
Efficacy of IL MMR and IL Vitamin D3 in Treatment of WartsMeasles, Mumps, Rubella VaccinePoor or no response1Participants
Efficacy of IL MMR and IL Vitamin D3 in Treatment of WartsVitamin D3Poor or no response1Participants
Number of Participants in Each Education Level GroupMeasles, Mumps, Rubella VaccineGraduate and higher2Participants
Number of Participants in Each Education Level GroupVitamin D3Graduate and higher4Participants

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMeasles, Mumps, Rubella Vaccine33
Overall StudySTARTEDVitamin D333
Overall StudyCOMPLETEDMeasles, Mumps, Rubella Vaccine31
Overall StudyCOMPLETEDVitamin D330
Overall StudyNOT COMPLETEDMeasles, Mumps, Rubella Vaccine2
Overall StudyNOT COMPLETEDVitamin D33

Adverse events12

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherPainSkin and subcutaneous tissue disordersMeasles, Mumps, Rubella Vaccine313131
otherPainSkin and subcutaneous tissue disordersVitamin D3303030
otherSwellingSkin and subcutaneous tissue disordersMeasles, Mumps, Rubella Vaccine0310
otherSwellingSkin and subcutaneous tissue disordersVitamin D3183018
otherPruritusSkin and subcutaneous tissue disordersMeasles, Mumps, Rubella Vaccine1311
otherPruritusSkin and subcutaneous tissue disordersVitamin D35305
otherHyperpigmentationSkin and subcutaneous tissue disordersMeasles, Mumps, Rubella Vaccine1311
otherHyperpigmentationSkin and subcutaneous tissue disordersVitamin D39309
otherHypopigmentationSkin and subcutaneous tissue disordersMeasles, Mumps, Rubella Vaccine2312
otherHypopigmentationSkin and subcutaneous tissue disordersVitamin D32302

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMeasles, Mumps, Rubella Vaccine031
Total, all-cause mortalityVitamin D3030
Total, other adverse eventsMeasles, Mumps, Rubella Vaccine3131
Total, other adverse eventsVitamin D33030
Total, serious adverse eventsMeasles, Mumps, Rubella Vaccine031
Total, serious adverse eventsVitamin D3630

Papers32

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
2271835BACKGROUNDPubMed
2850861BACKGROUNDPubMed
3880029BACKGROUNDPubMed
8687332BACKGROUNDPubMed
15897380RESULTPubMed
15987315RESULTPubMed
16127954BACKGROUNDPubMed
16497887BACKGROUNDPubMed
17210977BACKGROUNDPubMed
18472063BACKGROUNDPubMed

1 to 10 of 32

See all 32 papers

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons2

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Measles, Mumps, Rubella Vaccine vs Vitamin D3: deaths from any causeTrial comparisons
Measles, Mumps, Rubella Vaccine vs Vitamin D3: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04428359

GET https://conductscience.org/api/trials/v1/NCT04428359/results?page=2