FindTrial
Sign In

Subcutaneous infiltration of local anesthetic for postoperative pain following breast surgery

Portal blocks for postoperative pain relief in patients undergoing breast surgery-A Case Control Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070960
Enrollment
56
Registered
2024-07-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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: - Health Condition 3: C509- Malignant neoplasm of breast of unspecified site

Interventions

Intervention1: PORTAL BLOCKS FOR POSTOPERATIVE PAIN RELIEF IN PATIENTS UNDERGOING BREAST SURGERY: Subcutaneous injection of mixture of 8ml Injection 0.125% Bupivacaine + 1ml Triamcinolone 40mg + 1ml I

Sponsors

Namratha.M
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)ASA Grade 1,2 2)Age between 30-70 years 3)Female patients undergoing breast surgery

Exclusion criteria

Exclusion criteria: 1)Patient Refusal 2) ASA III and above 3) Patient with Coagulation disorders or on anticoagulant and antiplatelet drugs 4) Infection at the site of injection 5) Known allergy to the any of study drugs

Design outcomes

Primary

MeasureTime frame
To evaluate efficacy of portal blocks for post-operative pain management in woman undergoing Breast surgeryTimepoint: 20minutes after block, followed by every 2 hourly upto 48 hours—

Secondary

MeasureTime frame
To Evaluate patient satisfaction & effects on hemodynamic parametersTimepoint: starting from 20 minutes after the block, followed by every 2 hours for 48hours post surgery—

Countries

India

Contacts

Public ContactRavi Kerur

Jawaharlal Nehru Medical College

dr.namratha336@gmail.com8971747075

Outcome results

None listed

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