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An assessment about the effect of Pregabaline(75 mg) or Deuloxetin(30 mg) on pain relief in CPD due to Endometriosis

Comparison between the effect of oral Pregabalin (75 mg) and Deuloxetin (30mg) with Amitryptilin) on decreasing chronic pelvic pain due to Endometriosis

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015042916325N2
Enrollment
100
Registered
2015-06-26
Start date
2016-03-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Inflammatory disease of uterus, except cervix. Chronic inflammatory disease of uterus

Interventions

Intervention 1: Pregabalin 75 mg + Amitryptiline 10 mg. Intervention 2: Duloxetin 30 mg + Amitryptiline 10 mg.
Treatment - Drugs
Pregabalin 75 mg + Amitryptiline 10 mg
Duloxetin 30 mg + Amitryptiline 10 mg

Sponsors

Vice Chancellor for Research-Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Known case of Endometriosis according to pathology or radiology; Pelvic pain more than 6 month; Age between 18 and 60 years old; Comprehension and sign the consent inform. Exclusion Criteria: Previous surgery; Need to strong opioids; coexisting pelvic disorders; History of urinary tract infection,IBS, IBD, and cancer; Pregnancy and breast feeding; Psychiatric disorders(Minor and Major Depression, suicide, Bipolar disorders; Epilepsy; Hypertension; Hypersensitivity to drugs; MAOI consumption; Closed angle Glocoma; Renal Disorders; History of Juindice or hepatic disorders; Consumption of MAOI, SMRIs, SSRIs 2 weeks ago; Alcohol consumption; Hyponatremia; Weight gain>285 Pound

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain Score of Chronic pelvic pain due to Endometriosis. Timepoint: 2 weeks, 1 month, and 3 months after receiving the first dose of drug. Method of measurement: Numerical Rating Scale(NRS).

Secondary

MeasureTime frame
Severity of Chronic pelvic pain due to Endometriosis. Timepoint: 2 weeks, 1 month, and 3 months after receiving the first dose of drug. Method of measurement: With the question: How much do you experience pain relief after receiving treatment from our center? (0-100%).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKatayoun Haryalchi

Guilan University of Medical Sciences

k_haryalchi@yahoo.com+98 133228724

Outcome results

None listed

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