Darwish Hymenotomy Technique in Cases of Postpubertal Imperforate Hymen

NCT04661098 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2020-12-09

No results posted yet for this study

Summary

This study aims to test the use of a 10 mm laparoscopy trocar tip for formation of a new vaginal orifice with preservation of an annular hymen (Darwish hymenotomy technique) in cases of post pubertal imperforate hymen (IH). A prospective interventional case series done at a minimally invasive surgery unit of a tertiary university hospital between July 2013 and October 2019 comprising patients with primary amenorrhea and hematocolpus. Circular hymenotomy using a 10 mm laparoscopy trocar tip and sleeve done under general anesthesia was done in 36 cases. Documented vaginal patency with formation of an annular hymen in all cases was reported on follow-up visits without reported intraoperative complications. Patient and family satisfaction with excellent sensation of preserved hymen was also documented. Using a 10 mm laparoscopy trocar tip for formation of a new vaginal opening with preservation of annular hymen (Darwish technique) in cases of postpubertal IH is a simple, effective and safe procedure suitable for Islamic and conservative societies with excellent impact on the psychological and emotional status of the patient and her family.

Conditions

  • Imperforate Hymen

Interventions

PROCEDURE

(Darwish hymenotomy technique)

Formation of an annular hymen in cases of postpubertal imperforate hymen using a laparoscopic trocar (Darwish hymenotomy technique)

Sponsors & Collaborators

  • Professor Atef Darwish

    lead OTHER

Principal Investigators

  • Atef Darwish · Woman's Health University Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
12 Years
Max Age
15 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2019-09-30
Completion
2019-10-31

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Read the full study record

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View NCT04661098 on ClinicalTrials.gov