FindTrial
Sign In

To study the effect of different concentrations of local anesthetic on pain control when given in regional anesthesia (erector spinae plane block)for breast surgery

Comparative evaluation of analgesic efficacy of different concentrations of Levobupivacaine In Ultrasound Guided Erector Spinae Block For Breast Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/11/029140
Enrollment
60
Registered
2020-11-16
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: O- Medical and Surgical

Interventions

Intervention1: 0.375% levobupivacaine: 20ml of0.375% %levobupivacaine will be given before induction with standard general anesthesia technique.postoperative analgesia will be assessed Control Interv

Sponsors

DrKewal Krishan Gupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I AND II PATIENTS PATIENTS SCHEDULED FOR BREAST SURGERY

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
QUALITY OF ANALGESIATimepoint: in postoperative period at 0,2â??4â??8â??12â??18â??24hours—

Primary

MeasureTime frame
TOTAL DURATION OF ANALGESIA WILL BE NOTED IN TWO GROUPS POSTOPERATIVELY .IT WILL BE TAKEN FROM TIME OF COMPLETION OF INJECTION TO THE REQUEST OF FIRST RESCUE ANALGESIATimepoint: In the first 24 hours of postoperative period—

Countries

India

Contacts

Public ContactDr sarvjeet kaur

BFUHS

doc_krishan31@yahoo.co.in9988316306

Outcome results

None listed

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