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Comparison of the effect of arterial carbon dioxide pressure and nausea, vomiting and pain after laparoscopic cholecystectomy

Comparison of the effect of arterial carbon dioxide pressure and nausea, vomiting and pain after laparoscopic cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141209020258N185
Enrollment
60
Registered
2023-05-30
Start date
2023-06-06
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Laparoscopic cholecystectomy. Retained cholelithiasis following cholecystectomy

Interventions

Intervention 1: The first intervention group: in one group, patients will receive standard CO2 gas pressure (14-15 mmHg) during surgery. Intervention 2: The second intervention group: In the second gr

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age: 18 to 65 years old ASA class I and II Candidate for laparoscopic cholecystectomy surgery No chronic use of narcotics, NSAIDs and benzodiazepines

Exclusion criteria

Exclusion criteria: Changing laparoscopic surgery to open surgery Extending the operation time more than 3 hours The need for blood transfusion during the operation Dissatisfaction to continue attending the study

Design outcomes

Primary

MeasureTime frame
Arterial blood gas. Timepoint: The beginning of the action and the end of the action. Method of measurement: Blood test.;Nausa. Timepoint: From the time of entering recovery and every 15 minutes to one hour and 2, 4, 8, 12 and 24 hours after surgery. Method of measurement: Physical examination.;Vomitting. Timepoint: From the time of entering recovery and every 15 minutes to one hour and 2, 4, 8, 12 and 24 hours after surgery. Method of measurement: Physical examination.;Pain. Timepoint: Recovery and 4 hours after surgery. Method of measurement: Visual analog scale of pain.;Mean Ondansetron. Timepoint: At the end of the study. Method of measurement: Physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Hesamedin Modir

Arak University of Medical Sciences

modir.he@gmail.com+98 86 3222 2003

Outcome results

None listed

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