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Evaluation of effectiveness of blocking nerve supply to breast and axilla intraoperatively for post operative pain relief after breast surgery

Evaluation of effectiveness of modified Pec II block for post operative pain relief after breast surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/03/008209
Enrollment
60
Registered
2017-03-27
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: null- Breast cancer patients

Interventions

Intervention1: intervention- 0.2% ropivacaine : Pec I block is given( 10 ml of 0.2 % ropivacaine ) between the pectoralis major and pectoralis minor and Pec II block beneath pectoralis minor at the le

Sponsors

Dr Mary Thomas
Lead Sponsor
Dr Frenny Ann Philip
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. All ASA PS 1& 2 patients posted for modified radical mastectomy and breast conservative surgery 2. Patients with stage I, II, III disease 3. No residual Disease at end of surgical resection

Exclusion criteria

Exclusion criteria: •Local anaesthetic allergy •BMI >40 Kg/ m2 and •Fungating breast •Bleeding dyscrasias and patients on anticoagulants •Tumor infiltrating chest wall •Diabetic neuropathy •Patients on anticonvulsants •Chemotherapy induced peripheral neuropathy •Neurologic deficits

Design outcomes

Primary

MeasureTime frame
-Once patient is awake the patient is asked about pain (NRS score) and need for analgesics is assessed -Need for analgesia in Recovery room -If analgesics not required previously time of first demand of analgesics in HDU : Timepoint: 1 hour after surgery is again asked about pain with rest and movement ( NRS score) and need for analgesics. Once shifted to post operative ward and the time to request for first dose of analgesic is assessed if analgesics not requested till then. Post operatively patient will be again assessed at 6, 12,18 and 24 hours on NRS score both at rest and movement.

Secondary

MeasureTime frame
Total amount of analgesics required for patient to be comfortable Complications if any Post operative nausea vomiting Timepoint: 24 hours

Countries

India

Contacts

Public ContactDrFrenny Ann Philip

RCC

frennyp@gmail.com9495430286

Outcome results

None listed

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