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Effect of different pulmonary recruitment manoeuvre pressures on post-laparoscopic shoulder pain

A randomized controlled double blind trial comparing effect of different pulmonary recruitment manoeuvre pressures on post-laparoscopic shoulder pain - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063927
Enrollment
168
Registered
2024-03-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: K804- Calculus of bile duct with cholecystitis Health Condition 2: K358- Other and unspecified acute appendicitis Health Condition 3: K420- Umbilical hernia with obstruction,without gangrene

Interventions

Intervention1: pulmonary recruitment maneouvre (PRM) for post-laparoscopic shoulder pain: Group I will receive PRM pressure of 20cmH2O Group II will receive PRM pressure of 40cmH2O Control Interventi

Sponsors

Dr Nithu Dina Joseph
Lead Sponsor
Dr Shweta Konnur
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: ASA I and II patients posted for laparoscopic surgeries under GA of duration upto 4 hours

Exclusion criteria

Exclusion criteria: Patient refusal to participate in study, BMI more than 30, patients with chronic shoulder pain, history of previous shoulder surgery, COPD/respiratory pathologies, patients with hemodynamic instability, high intracranial pressure and right heart failure, pregnancy

Design outcomes

Primary

MeasureTime frame
To compare the effect of two different pulmonary recruitment manoeuvre pressures on intensity of post-laparoscopic shoulder painTimepoint: post operative hemodynamic assessment at 1 min, 3min and 5 mins after the maneouvre is performed, followed by vas score, total analgesia consumption and side effect assessment postoperatively upto 24 hours (every 2 hours for first 12 hours, every 6 hours for next 12 hours)—

Secondary

MeasureTime frame
Hemodynamic parameters before and after PRMTimepoint: Intra-operatively before PRM and 1,3 and 5 mins after PRM;side effects like nausea and vomitingTimepoint: post-operatively upto 24 hours;Total consumption of analgesics in 24 hours in all groupsTimepoint: post-operatively upto 24 hours—

Countries

India

Contacts

Public ContactDr Nithu Dina Joseph

Bharati Vidyapeeth Deemed to be University

shwetajm81@gmail.com9823890369

Outcome results

None listed

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