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Continous perineural erector spinae block for modified radical mastectomy: A clinical trial

Is continous perineural erector spinae block really necessary in patients undergoing modified radical mastectomy for achieving optimal post operative analgesia?: A prospective, randomized, controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062203
Enrollment
60
Registered
2024-02-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: ULTRASOUND GUIDED ESP BLOCK single bolus: ESP block SINGLE BOLUS with Inj bupivacaine 0.25% 30ml with dexamethasone 4mg and assess post-op analgesia for 48 hours Control Intervention1:

Sponsors

Dr Manvi Katoch
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA-1&2 BMI- 18.5-29.9 kg/m2

Exclusion criteria

Exclusion criteria: ASA 3&4 any history of local anesthetic allergy refusal for nerve block

Design outcomes

Primary

MeasureTime frame
To compare postoperative analgesia duration in both groups for 48 hours.Timepoint: Patients will be assessed for pain using VAS scale after every 2 hours till 8 hours & then every 4 hours till 48 hours postoperatively—

Secondary

MeasureTime frame
a)to compare patient satisfaction score in both groups b)adverse effects if anyTimepoint: total number of rescue doses consumed in 48 hours—

Countries

India

Contacts

Public ContactDr Manvi Katoch

Dr RPGMC Tanda

anitasharma677@gmail.com9418921676

Outcome results

None listed

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