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We compare continuous infusion and intermittent bolus infusion post operative patient-controlled analgesia with erector spinae block catheter

Comparison of continuous infusion and intermittent bolus infusion for postoperative patient-controlled analgesia with erector spinae block catheter: a randomized, double- blind, controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033759
Enrollment
30
Registered
2021-05-24
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

Interventions

Intervention1: Group 1 :Ropivacaine will be given as a bolus of 10 mL every hour over 80 s.: 0.2% Ropivacaine will be given as a bolus of 10 mL every hour in the interfascial plane between: erector

Sponsors

AIIMS Patna
Lead Sponsor
Dr Chandni Sinha
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: ASA I/II female patients scheduled for unilateral MRM under general anaesthesia

Exclusion criteria

Exclusion criteria: Patients unable to cooperate or give consent Known allergy to local anesthetic, non-steroidal anti-inflammatory drugs or opioids, Infection at the injection site, Coagulopathy

Design outcomes

Primary

MeasureTime frame
Assess the consumption of local anesthetic during PCA in 24 hoursTimepoint: 24 hour—

Secondary

MeasureTime frame
1.Numerical rating scores (NRS) 2.the frequency of PCA use 3.patient satisfaction 4. side effects Timepoint: 24 hours—

Countries

India

Contacts

Public ContactDr Chandni Sinha

AIIMS Patna

chandni.doc@gmail.com7250333148

Outcome results

None listed

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