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NCT02218463 · ClinicalTrials.gov registry record · NA
Treatment of Prepubertal Labial Adhesions
A NA study, sponsored by Children's Mercy Hospital Kansas City.
- Completed
- Registry status
- NA
- Development phase
- 43
- Enrollment target
NCT02218463 is a NA study that has completed, run by Children's Mercy Hospital Kansas City. The registered enrollment target is 43 participants.
The verdict
NCT02218463, a NA study, has completed, sponsored by Children's Mercy Hospital Kansas City.
- COMPLETED
- Registry status
- NA
- Development phase
- 43 participants
- Enrollment target
Study Summary
First-line treatment for labial adhesions in prepubertal girls has been topical estrogen. This study aims to evaluate an alternative and less costly option of treatment with potentially less side effects. Primary Hypothesis: There will be a difference in complete resolution of labial adhesions with topical estrogen with lateral traction as compared to an emollient with lateral traction.
Interventions
- DRUG Cetaphil
- DRUG Estradiol cream 0.01%
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 43 participants |
| Start Date | 2014-09 |
| Est. Completion | 2016-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02218463
The ClinicalTrials.gov registry entry for NCT02218463 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 43 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Children's Mercy Hospital Kansas City, which has 184 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Cetaphil is the first listed.
NCT02218463 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02218463 about?
NCT02218463 is a clinical study titled "Treatment of Prepubertal Labial Adhesions". First-line treatment for labial adhesions in prepubertal girls has been topical estrogen. This study aims to evaluate an alternative and less costly option of treatment with potentially less side effects. Primary Hypothesis: There will be a difference in complete resolution of labial adhesions wit...
What is the current status of trial NCT02218463?
This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2014-09. Estimated completion is 2016-06.
What interventions are being tested in trial NCT02218463?
The interventions under investigation include: Cetaphil (DRUG), Estradiol cream 0.01% (DRUG).
Who is sponsoring clinical trial NCT02218463?
This trial is sponsored by Children's Mercy Hospital Kansas City, which has 184 total clinical trials registered on ClinicalTrials.gov.
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