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Trial · NCT04709484

Comparison of the Effectiveness of USG and Palpation Guidance Steroid Injection in Patients With Plantar Fasciitis

NCT04709484, Not applicable, Completed, Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey; results first posted 2021-10-20

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Comparison of the Effectiveness of USG and Palpation Guidance Steroid Injection in Patients With Plantar Fasciitis. Trials, record NCT04709484. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04709484

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Trial

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

Title
Comparison of the Effectiveness of USG and Palpation Guidance Steroid Injection in Patients With Plantar Fasciitis
NCT number
NCT04709484
Status
Completed
Phases
Not applicable
Enrollment
66 participants, actual
Lead sponsor
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
Conditions
Plantar Fasciitis
Interventions
USG-guided steroid injection, Palpation-guided steroid injection
First posted
2021-01-14
Last updated
2021-10-20
Results first posted
2021-10-20

Source ClinicalTrials.gov

Registered outcomes6

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

ListOutcomeTime frameDescription
PrimaryPain Severityday 0 (before intervention)visual analog scale (0-10) minimum score: 0 maximum score: 10. Higher scores reflect more severe pain. Higher values represent a worse outcome.
PrimaryPain Severity1 month after interventionvisual analog scale (0-10) minimum score: 0 maximum score: 10. Higher scores reflect more severe pain. Higher values represent a worse outcome.
PrimaryPain Severity3 month after interventionvisual analog scale (0-10) minimum score: 0 maximum score: 10. Higher scores reflect more severe pain. Higher values represent a worse outcome.
SecondaryFoot Function Indexday 0 (before intervention)
Foot Function Index(FFI) is a self-report questionnaire concerning foot function and pain. The FFI consists of 23 questions with scores 0-10 in three domains concerning foot pain, function and disability resulting in a total score range from 0 to 230. The score is validated for patients with plantar fasciitis with a minimal clinical important difference being 7 points. Higher values represent a worse outcome.
SecondaryFoot Function Index1 month after intervention
Foot Function Index(FFI) is a self-report questionnaire concerning foot function and pain. The FFI consists of 23 questions with scores 0-10 in three domains concerning foot pain, function and disability resulting in a total score range from 0 to 230. The score is validated for patients with plantar fasciitis with a minimal clinical important difference being 7 points. Higher values represent a worse outcome.
SecondaryFoot Function Index3 month after intervention
Foot Function Index(FFI) is a self-report questionnaire concerning foot function and pain. The FFI consists of 23 questions with scores 0-10 in three domains concerning foot pain, function and disability resulting in a total score range from 0 to 230. The score is validated for patients with plantar fasciitis with a minimal clinical important difference being 7 points. Higher values represent a worse outcome.

Outcomes6

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPain Severityday 0 (before intervention)intent to treat population(all participants)score on a scaleMEAN
PRIMARYPain Severity1 month after interventionintent to treat population(all participants)score on a scaleMEAN
PRIMARYPain Severity3 month after interventionintent to treat population(all participants)score on a scaleMEAN
SECONDARYFoot Function Indexday 0 (before intervention)intent to treat population(all participants)score on a scaleMEAN
SECONDARYFoot Function Index1 month after interventionintent to treat population(all participants)score on a scaleMEAN
SECONDARYFoot Function Index3 month after interventionintent to treat population(all participants)score on a scaleMEAN

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
Pain SeverityUSG-guided Steroid Injection Group8.50Standard Deviation 0.90score on a scale
Pain SeverityPalpation-guided Steroid Injection Group8.31Standard Deviation 0.90score on a scale
Pain SeverityUSG-guided Steroid Injection Group1.50Standard Deviation 1.83score on a scale
Pain SeverityPalpation-guided Steroid Injection Group1.53Standard Deviation 2.29score on a scale
Pain SeverityUSG-guided Steroid Injection Group1.44Standard Deviation 2.08score on a scale
Pain SeverityPalpation-guided Steroid Injection Group1.75Standard Deviation 2.46score on a scale
Foot Function IndexUSG-guided Steroid Injection Group65.41Standard Deviation 12.78score on a scale
Foot Function IndexPalpation-guided Steroid Injection Group63.78Standard Deviation 13.80score on a scale
Foot Function IndexUSG-guided Steroid Injection Group8.06Standard Deviation 13.46score on a scale
Foot Function IndexPalpation-guided Steroid Injection Group7.47Standard Deviation 13.66score on a scale

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDUSG-guided Steroid Injection Group34
Overall StudySTARTEDPalpation-guided Steroid Injection Group32
Overall StudyCOMPLETEDUSG-guided Steroid Injection Group34
Overall StudyCOMPLETEDPalpation-guided Steroid Injection Group32
Overall StudyNOT COMPLETEDUSG-guided Steroid Injection Group0
Overall StudyNOT COMPLETEDPalpation-guided Steroid Injection Group0

Adverse events0

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

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityUSG-guided Steroid Injection Group00
Total, all-cause mortalityPalpation-guided Steroid Injection Group00
Total, other adverse eventsUSG-guided Steroid Injection Group00
Total, other adverse eventsPalpation-guided Steroid Injection Group00
Total, serious adverse eventsUSG-guided Steroid Injection Group00
Total, serious adverse eventsPalpation-guided Steroid Injection Group00

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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 comparisons0

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

None in this release.

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/NCT04709484

GET https://conductscience.org/api/trials/v1/NCT04709484/registered