Investigating the effect of anti-adhesion substances in reducing adhesion after laparoscopic endometriosis surgery

Investigating the effect of anti-adhesion substances in reducing adhesions after laparoscopic endometriosis surgery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20221121056562N1

Enrollment

Registered

2023-01-25

Start date

2023-02-19

Completion date

Unknown

Last updated

2023-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis. Endometriosis

Interventions

Intervention 1: Intervention group: During laparoscopic surgery for endometriosis, after releasing the adhesions and shaving the intestine, the anti-adhesion material (interguard oxidized regenerated

Eligibility

Sex/Gender

Female

Age

15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Women in the age group of 15 to 45 years Women diagnosed with infertility Women with chronic cyclic pelvic pain associated with menstruation Patients who are diagnosed with severe endometriosis (stage 3 and 4) according to clinical and ultrasound criteria.

Exclusion criteria

Exclusion criteria: Pregnancy Lactating lady Laparoscopy contraindications (coagulopathy - cirrhosis - unclear anatomy - heart - lung disease)

Design outcomes

Primary

Measure	Time frame
Abdominal adhesions. Timepoint: Three to six months after surgery. Method of measurement: Sonography , According to the scoring system Enzian.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShiva Mahmooudzadeh

Karaj University of Medical Sciences

shiva.kani91@gmail.com+98 26 3222 2021

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026