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comaprision of two techniques of serratus anterior plane block for pain releif after surgery for breast cancer.

Impact of Supra-Serratus versus Sub-Serratus variations of Serratus Anterior Plane Block for postoperative analgesia and quality of recovery after modified radical Mastectomy- a randomized control trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046517
Enrollment
70
Registered
2022-10-14
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: C509- Malignant neoplasm of breast of unspecified site Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: USG guided Sub-serratus regional block: A regional block using of ropivacaine 0.25% (30 mL will be used per side in patients weighing over 60 kg and 20 mL will be used in patients weigh

Sponsors

NIMS HospitalHyderabad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 70 adult patients of either gender aged more than or equal to 18 years classified under ASA 1,2 or 3 scheduled for modified radical mastectomy

Exclusion criteria

Exclusion criteria: 1. Any known sensory deficit of the anterolateral chest wall. 2. Any local infection at site of blockade. 3. Pregnancy 4. Allergy to amide local anesthetic medications 5. Chronic pain conditions 6. Preoperative opioid use greater than 20 oral morphine equivalents per day 7. Any coagulation abnormality which would be a contraindication for block placement 8. Body mass index >50 9. Refusal to participate in the study

Design outcomes

Primary

MeasureTime frame
Opioid consumption during the 24 hours following placement of the serratus anterior plane blockTimepoint: 6-12 hours postopertive 12-24 hours postopeartive—

Secondary

MeasureTime frame
Change in immediate post-operative pain scores from their pre-operative baseline 2. NRS Pain scores during the first 24 hours after placement of the block 3.Quality of recovery after surgery as assessed by the quality of recovery-15 questionnaire assessed at discharge from hospital.(7) 4. Patient satisfaction with regards to their perioperative pain control during the first 24 hours after placement of the block. 5. Presence of nausea or vomiting /any other adverse effect 7. Duration of sleep during the first post-operative night 8. Block performance time Timepoint: 0,6,12,18,24 hours postoperative—

Countries

India

Contacts

Public ContactShibani Padhy

Department of Anaesthesiology and intensive care, NIZAMS institute of medical sciences, Hyderabad

drshibanipadhy@gmail.com8332921975

Outcome results

None listed

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