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The comparison of treatment with dienogest and contraceptive oral pills on the improvement of pain, and quality of life in surgery patients with advanced endometriosis

The comparison of treatment with dienogest and contraceptive oral pills on the improvement of pain, and quality of life in surgery patients with advanced endometriosis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191011045063N1
Enrollment
108
Registered
2020-02-20
Start date
2019-03-21
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

Advanced endometriosis. Endometriosis

Interventions

Intervention 1: Intervention group: The first group will receive the dienogest drug. Dosage of one tablet of 2 mg daily for six months. Intervention 2: Intervention group: The second group will receiv

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Early diagnosis of endometriosis and chronic pelvic pain associated with endometriosis Patients with advanced endometriosis who underwent surgery Age 18 - 45 years Body mass index (BMI) 18.5 – 29.9 kg/m2; No gynecological malignancy No contraindications to OCP or dienogest No plans of pregnancy in the near No underlying diseases

Exclusion criteria

Exclusion criteria: Personal dissatisfaction for inclusion in the study Patients whose pelvic pain originates from other organs Use of gonadotropins or other hormones three months before surgery

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before surgery, 3 and 6 months after surgery. Method of measurement: Pelvic pain and dyspareunia scores are evaluated using the Visual Analogue Scale (VAS) and dysuria and dyschezia using a three-point score questionnire by possible answers to the items were “yes”, “no”, and “a little”.

Secondary

MeasureTime frame
Quality of life. Timepoint: Before surgery, 3 and 6 months after surgery. Method of measurement: Quality of life was measured using WHOQOL-BREF.;Edverse effects of the treatment. Timepoint: 3 and 6 months after surgery. Method of measurement: Questionnaire.;Pain recurrence. Timepoint: 6 months after surgery. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGelareh Niakan

Iran University of Medical Sciences

g.niakan59@gmail.com+98 21 8807 1886

Outcome results

None listed

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