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Effect of injectable triptrelin in patients with obsessive compulsive disorder

Effectiveness of adding injectable triptrelin to treatment regimen of patient with obsessive-compulsive disorder

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180309039012N1
Enrollment
30
Registered
2018-10-06
Start date
2018-04-05
Completion date
Unknown
Last updated
2018-11-05

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

Conditions

obsessive compulsive disorder. Obsessive-compulsive disorder

Interventions

Intervention 1: Intervention group: Injecting Tryptrolin 3.75 mg three times a day, at the beginning of the study and one month later and two months respectively. Intervention 2: Control group: Inject

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: diagnosis of obsessive-compulsive disorders based on DSM-V criteria aged 18-64 years completed consent form by he patient or his family at least eight grade education Obsessive-compulsive patients who have received at least eight weeks of adequate SSRI treatment and, if necessary, benzodiazepine or anti-psychotic that does not affect the level of the gonadal hormones And the yele Brown score is above 17

Exclusion criteria

Exclusion criteria: simultaneous psychiatric disorders liver disorders use of opioid substance other than cigarttes A hypersensitivity reaction or any untoward side effects caused by the drug use of other interfering drug Any contraindications for tryptorelin such as pregnancy or lactation or bone diseases that are taken from patients during the initial history. medical illness

Design outcomes

Primary

MeasureTime frame
Obsession compulsion symptoms in yel brown questionnaire. Timepoint: Before starting the study and at times, 0,1, 2 and 4 month after starting treatment. Method of measurement: obsession symptoms assessment questionnaire yele-brown.;Clinical symptoms of obsession. Timepoint: Before starting the study and at times, 0,1, 2 and 4 month after starting. Method of measurement: clinical interview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFaezeh Nikzad

Mashhad University of Medical Sciences

nikzadf941@mums.ac.ir+98 51 3894 5361

Outcome results

None listed

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