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treatment outcomes of dienogest versus elagolix in endometriosis

Comparative Effectiveness of Dienogest and Elagolix in Endometriosis: A Prospective Observational Study at a Tertiary Care Centre in Northern India - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101119
Enrollment
200
Registered
2026-01-14
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: N00-N99- Diseases of the genitourinary system

Interventions

Intervention1: Elagolix: dose 150 mg once a day orally for three months Intervention2: Elagolix 150 mg once day: Nil Intervention3: Nil: Nil Control Intervention1: Dienogest: Dose 2 mg once a day oral

Sponsors

University of Kashmir
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Female patients aged 18 to 45 years Diagnosed with endometriosis clinical or USG based VAS pelvic pain score equal or greater than 4 Willing to undergo 3 months of treatment and follow up Provided written informed consent

Exclusion criteria

Exclusion criteria: Hormonal therapy or surgery for endometriosis in past 3 months Significant hepatic renal or bone disease Pregnancy or lactation Other pelvic pathologies mimicking endometriosis

Design outcomes

Primary

MeasureTime frame
Decrease in pelvic pain score VASTimepoint: Three months after treatment

Secondary

MeasureTime frame
Quality of LifeTimepoint: three months after treatment;Uterine Volume Endometrioma Volume Fluid Cyst volumeTimepoint: three months after treatment;CA 125 levelsTimepoint: Three months after Treatment

Countries

India

Contacts

Public ContactDrGhulam Nabi Bader

Department of Pharmaceutical Sciences University of kashmir

syedaatir06@gmail.com9149650374

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026