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Cesarean Scar Healing Randomized Trial Compares Two Ointments

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Summary

This registry entry documents a randomized controlled trial (NCT07547462) comparing hydrophilic methacrylate gel versus beta-sitosterol ointment for early cesarean section scar healing. Adult women who underwent cesarean delivery were randomly assigned to receive either hydrophilic methacrylate gel (n=58) or beta-sitosterol ointment (n=59), with scar outcomes assessed by trained nurses blinded to treatment allocation at two time points approximately 12 days apart. The primary outcome is scar redness measured by the Vancouver Scar Scale, with secondary outcomes including pigmentation, pliability, scar height, pain, itching, satisfaction, and treatment recommendation.

“Adult women who underwent cesarean delivery were randomly assigned to receive either hydrophilic methacrylate gel (n=58) or beta-sitosterol ointment (n=59).”

NIH , verbatim from source
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About this source

ClinicalTrials.gov is the NIH-run registry of every clinical trial conducted in the United States, plus most international trials sponsored by US-based companies or institutions. By federal law, sponsors must register Phase 2 through Phase 4 studies before enrolling patients and post results within a year of completion. This feed tracks every new trial registration and study update, around 700 a month: drug interventions, device studies, behavioral protocols, observational research. Watch this if you scout drug candidates moving into mid or late-stage development, monitor competitor pipelines, or follow rare disease research where new trials signal patient hope. GovPing parses sponsor, phase, intervention, and target indication on each entry.

What changed

This ClinicalTrials.gov registry entry describes an randomized controlled trial comparing two topical agents for early cesarean section scar healing. Hydrophilic methacrylate gel (n=58) is compared against beta-sitosterol ointment (n=59), with blinded nurse assessment of the primary outcome (Vancouver Scar Scale redness) at two visits approximately 12 days apart. Secondary endpoints include pigmentation, pliability, scar height, pain, itching, satisfaction, and treatment recommendation. This entry documents the trial design and registration status; it does not report efficacy results.

Affected parties include clinical investigators conducting wound-healing and obstetrics research, and manufacturers of topical wound-care or scar-treatment products who may wish to monitor comparative effectiveness data. Sponsors considering similar scar-treatment development programs should note the trial design and outcome measures as a benchmark for future study design.

Archived snapshot

Apr 23, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← ClinicalTrials.gov Studies

Optimizing Early Cesarean Scar Healing

N/A NCT07547462 Kind: NA Apr 23, 2026

Abstract

This randomized controlled trial compares hydrophilic methacrylate gel versus beta-sitosterol ointment for early cesarean section scar healing. Adult women who underwent cesarean delivery were randomly assigned to receive either hydrophilic methacrylate gel (n=58) or beta-sitosterol ointment (n=59). Scar outcomes were assessed by trained nurses blinded to treatment allocation and by patients at two time points approximately 12 days apart. The primary outcome was scar redness measured by the Vancouver Scar Scale. Secondary outcomes included pigmentation, pliability, scar height, and patient-reported measures including pain, itching, satisfaction, and treatment recommendation.

Conditions: Cesarean Section Scar, Wound Healing

Interventions: Beta-Sitosterol Ointment, Hydrophilic Methacrylate Gel

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Last updated

Classification

Agency
NIH
Published
April 23rd, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Clinical investigators
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Pharmaceutical research Scar treatment
Geographic scope
United States US

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Clinical Operations
Topics
Healthcare Medical Devices

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