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Assessment of various volumes of local anaesthestic in interfascial plane blocks for breast surgery

Volume study of superficial serratus plane block for breast surgeries: a prospective randomized study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085901
Enrollment
36
Registered
2025-04-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: superficial serratus plane block: different volume studies Intervention2: volume studies of superficial serratus plane block: assessment of pain over 24 hours using 0.2% ropivacaine usi

Sponsors

Ruby hall clinic
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All adult female patients for elective surgery under general anaesthesia coming under physical status ASA1 and 2.

Exclusion criteria

Exclusion criteria: No consent and cooperation for the procedure, Allergy to any drugs used in the study, Weight less than 50 kg or obesity bmimore than 35kg per m Liver disease, renal disease, arrhythmia Chronic pain Neuromuscular disease Pregnancy

Design outcomes

Primary

MeasureTime frame
Assessment of volume in analgesic efficacy of superficial serratus plane block in breast surgeryTimepoint: ANALGESIC EFFECT ACCESSED AT 0, 3, 6,12,18,24 HOURS.—

Secondary

MeasureTime frame
Adverse events & their role in chronic painTimepoint: AFTER 1 WEEK AND 3 MONTHS OF SURFERY—

Countries

India

Contacts

Public ContactNita DSouza

Ruby hall clinic

drnita610@yahoo.com9823721982

Outcome results

None listed

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