To Assess The Effect Of Preoperative Transcranial Magnetic Stimulation On Post Surgical Pain After Breast Surgery
- Conditions
- Health Condition 1: C50-C50- Malignant neoplasms of breast
- Registration Number
- CTRI/2024/08/072404
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Age 18-70 years,
2. American Society of Anaesthesiologists (ASA) physical status I-III,
3. Scheduled for elective surgery for breast cancer (unilateral surgical procedure with or without axillary lymph node dissection).
1. Patient refusal,
2. Contraindications to transcranial magnetic stimulation:
iii.Patients who have ferromagnetic or magnetic sensitive metal objects implanted in the head or neck areas in close proximity to the TMS coil magnetic fields.
iv.Surgical placement of medical devices (eg, metal plates, clips, electrodes, chips, pumps, stimulators, cochlear implants, pacemakers), as well as past exposure to all metal fragments, tattoos rendered with ferromagnetic-containing ink, permanent piercings, and/or other possible metal sources in the head and neck.
3. Neurological or psychiatric disorders, concurrent major depression,H/o head trauma
4. History of substance abuse,
5. ASA-PS IV or more,
6. History of Head trauma.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the reduction in incidence of PMPS using SF-MPQ and EQ-5D-3L questionnaire.Timepoint: at 3 months
- Secondary Outcome Measures
Name Time Method Secondary outcomes include assessment of postoperative opioid consumption up to 24 hrs and postoperative pain assessment up to 24 hours using Numeric Pain Rating Scale (NRS).Timepoint: up to 24 hours in post-operative period