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A clinical trial to study the effect of negative aspiration of pneumoperitoneum over shoulder tip pain during laparoscopic removal of gallbladder : Randomized Control Trial Study

Effect of active aspiration of pneumoperitoneum on shoulder-tip pain following laparoscopic cholecystectomy: a randomized controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102161
Enrollment
40
Registered
2026-01-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: K801- Calculus of gallbladder with othercholecystitis

Interventions

Intervention1: Effect of active aspiration of pneumoperitoneum on shoulder-tip pain following laparoscopic cholecystectomy: Following completion of the laparoscopic cholecystectomy,in the treatment gr

Sponsors

Department of General Surgery AIIMS Deoghar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients with chronic calculous cholecystitis of American Society of Anesthesiology Grade (ASA) 1 or 2

Exclusion criteria

Exclusion criteria: All Previous abdominal surgery Patient getting converted from laparoscopic to open surgery intraoperatively. Patient receiving abdominal drains post operatively. Pregnant patients Patients with acute or acute on chronic calculous cholecystitis. Patient unfit for pneumoperitoneum. Active Sepsis or Coagulopathy. Patient not able to understand the visual analogue scale Patient not consenting for surgery

Design outcomes

Primary

MeasureTime frame
To compare the difference in the shoulder pain and abdominal pain scores between the passive (control) and active (intervention) pneumoperitoneum-aspiration groups.Timepoint: In the post-operative period, right shoulder pain and abdominal pain will be noted using Visual Analogue Scale (VAS) at 4 hourly SOS for Next 48 hours post-operatively.—

Secondary

MeasureTime frame
To compare the difference between analgesic requirements in between the two groups.Timepoint: Patients of both groups will receive 12 hourly analgesia of intravenous (IV) diclofenac sodium injection (75 mg) for first 24 hour followed by as per need analgesia after 24 hours. In this period of 48 hours, patient may receive additional analgesics if needed (75 mg IV diclofenac sodium injection or IV paracetamol 1 gram 50 mg intramuscular (IM) Tramadol) by the patient on SOS basis. Total dose and the types of analgesics given will be noted for each patient for this 48-hour duration.—

Countries

India

Contacts

Public ContactDr Abhinav Prakash Arya

AIIMS Deoghar

abhinavapa@gmail.com8601364363

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026