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Comparison of two different nerve blocks for post operative pain in modified radical mastectomy patients: A double blinded randomized trial

Comparison of mid-point transverse process to pleura (MTP) block and Erector spinae plane block for post-operative pain in modified radical mastectomy patients: A double blinded randomized trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034133
Enrollment
66
Registered
2021-06-10
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: C509- Malignant neoplasm of breast of unspecified site Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: mid transverse process to pleura block: Group 1 patients will receive MTP block at T3 or 4 level unilaterally on the operative side.patients will receive 20 ml ropivacaine 0.5%. Control

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1, 2 and 3 Scheduled to undergo MRM

Exclusion criteria

Exclusion criteria: 1. Patient refusal 2. Preexisting infection at block site 3. Coagulation Disorder 4. Preoperative hypotension (Mean arterial blood pressure 5. History of psychiatric illness and preexisting neurological deficits 6. Patient with morbid obesity BMI >40 kg m2 7. Pregnant patients 8. Decreased pulmonary reserve, cardiac disorders and renal dysfunctions 9. Known allergy to study drugs 10. Patient with fungating growth or growth with infection at site of block 11. Patient posted for repeat surgery. 12. Presence of any preoperative pain or history of chronic pain 13. History of regular analgesic use 14. History of pre operative radiotherapy and chemotherapy.

Design outcomes

Primary

MeasureTime frame
The primary outcome of our study will be to assess visual analogue scale in post operative period for 24 hours.Timepoint: The primary outcome of our study will be to assess visual analogue scale in post operative period for 24 hours.—

Secondary

MeasureTime frame
The secondary outcome will be to assess and compare duration of analgesia (time to use first rescue analgesic), total amount of rescue analgesic used during 24 hours, duration to perform block, incidence of procedure related complications and postoperative complications, failure rate and patient satisfaction.Timepoint: analgesia for next 24 hours at 1hr, 2hr,3 hr,4hr,8hr,12hr,16hr,20 hr and 24 hr post operatively. satiafcation scors at 24 hours post operatively.—

Countries

India

Contacts

Public ContactPriyanka Sethi

AIIMS,Jodhpur.

dr.priyanka_sethi@yahoo.co.in

Outcome results

None listed

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