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Effect of Adjuvant Continuous Theta Burst Transcranial Magnetic Stimulation in Obsessive-Compulsive Disorder and comparison with Placebo magnetic stimulation.

Efficacy of adjunctive Continuous Theta Burst Transcranial magnetic stimulation in Obsessive-compulsive disorder: A Randomized placebo controlled study. - CTBSOCD

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/025881
Enrollment
36
Registered
2020-06-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: F42- Obsessive-compulsive disorder

Interventions

Intervention1: Continuous Theta Burst Transcranial Magnetic Stimulation: Continuous Theta Burst from a figure of eight coil (MCF - B65) using a TMS Machine (MagVenture - MagPro - R30) is applied on FP

Sponsors

Shri Guru Ram Rai Institute of Medical and Health Sciences and Shri Mahant Indresh Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosis of OCD, according to International Classification of Diseases â?? 10 Classification of Mental and Behavioural Disorders: Diagnostic Criteria for Research (ICD-10 DCR). 2. Moderate to severe illness. Baseline Y-BOCS Score > or equal to 24. 3. Age between 18-59 years. 4. Right handed, normotensive patients.

Exclusion criteria

Exclusion criteria: 1. Neurological disorders such as epilepsy, organic brain damage or any neurological procedures. 2. Pacemakers or other metal parts in the body. 3. ECT in past 6 months. 4. Any co morbid psychosis (F20-F29), Bipolar disorder or substance use disorders except nicotine and caffeine.

Design outcomes

Primary

MeasureTime frame
Yale Brown Obsessive Compulsive Scale (Y-BOCS)Timepoint: To be Measured at 0, 7 and 21 days of transcranial magnetic stimulation (3 Point Rating).

Secondary

MeasureTime frame
Hamilton Anxiety Rating Scale (HAM-A), Hamilton Depression Rating Scale (HAM-D) and Clinical Global Impression (CGI).Timepoint: To be Measured at 0, 7 and 21 days of transcranial magnetic stimulation (3 Point Rating).

Countries

India

Contacts

Public ContactParth Datta

Shri Guru Ram Rai Institute of Medical and Health Sciences

shobit.garg@gmail.com8958534261

Outcome results

None listed

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