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Trial · NCT06633185

Effect of Phenytoin Cream on Wound Healing After Anal Fissure Surgery.

NCT06633185, Phase 1, Completed, Mansoura University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effect of Phenytoin Cream on Wound Healing After Anal Fissure Surgery. Trials, record NCT06633185. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06633185

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Trial

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

Title
Effect of Phenytoin Cream on Wound Healing After Anal Fissure Surgery.
NCT number
NCT06633185
Status
Completed
Phases
Phase 1
Enrollment
50 participants, actual
Lead sponsor
Mansoura University
Conditions
Anal Fissure Chronic, Anal Fissure, Wound Healing
Interventions
phenytoin cream, no phenytoin cream
First posted
2024-10-09
Last updated
2024-10-09

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryThe duration of healing of anal fissure.21 to 30 daysThe primary endpoint will be the duration of healing of anal fissure in days. It will be defined as complete epithelization of the anal wound.
Secondarypost operative complications and others14 to 21 days
Postoperative analgesic requirements including whether the patient required additional opioids. It is measured by number of analgesic injections needed. Immediate post-operative complications e.g anal bleeding or urine retention. It is measured by number of cases which developed these complications Time taken to return to daily activities in days. Time taken for the patient to defecate without pain in days .

Outcomes0

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

None in this release.

Results by group0

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

None in this release.

Participant flow0

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

None in this release.

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 totals0

The totals the trial posted for each group.

None in this release.

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/NCT06633185

GET https://conductscience.org/api/trials/v1/NCT06633185/registered