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Comparison Between Oral Gabapentin and Pectoral Block for Pain Management in Patients Undergoing Breast Surgery

"Comparative study of USG guided pectoral blocks versus efficacy of preoperative oral gabapentin for post operative analgesia in patients undergoing breast surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/019374
Enrollment
105
Registered
2019-05-27
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: - Health Condition 2: D059- Unspecified type of carcinoma in situ of breast

Interventions

Intervention1: pectoral blocks: USG guided pectoral blocks will be given to look for post operative analgesia. total of 20ml 0.375% ropivacaine will be injected as pectoral blocks in two planes using

Sponsors

DR RAM MANOHAR LOHIA INSTITUTE OF MEDICAL SCIENCES LUCKNOW
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients giving consent 2. Females ages 30-65 undergoing breast surgery 3. ASA physical status I and II

Exclusion criteria

Exclusion criteria: 1. patients who do not give consent 2. patients on anticoagulant therapy 3. ASA status > II 4. patients having chest wall deformity or local site infection 5. allergic to local anaesthetics 6. serious neurological amd psychaitric disorders 7. patients already on gabapentin or other anticonvulsant 8. hepatic or renal dysfunction

Design outcomes

Primary

MeasureTime frame
1. intensity of pain at 2 hourly intervals for first 24 hours post operatively using VAS score 2. time of rescue analgesiaTimepoint: 2 hourly interval for first 24 hours in post operative period—

Secondary

MeasureTime frame
1. Intraoperative and postoperative hemodynamic changes 2. Evaluating adverse effects of Gabapentin like nausea, vomiting, sedation 3. Total analgesic consumption upto 24 hours after surgeryTimepoint: intraoperative and postoperatively for 24 hours—

Countries

India

Contacts

Public ContactDR PARUL SHARMA

DR. RAM MANOHAR LOHIA INSTITUTE OF MEDICAL SCIENCES

mamtaharjaidoctor@yahoo.co.in

Outcome results

None listed

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