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Anesthesia in laparoscopic cholecystectomy

Comparison of intraoperative blood pressure and heart rate changes, postoperative nausea, vomiting and pain in two methods of epidural and general anesthesia in laparoscopic cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201305289229N3
Enrollment
66
Registered
2013-06-17
Start date
2013-05-25
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: intraoperative hemodynamic changes. Condition 2: postoperative naseau and vomiting. Condition 3: postoperative pain. Other postprocedural disorders of circulatory system, not elsewhere classified Vomiting following gastrointestinal surgery Other postprocedural disorders of digestive system, not elsewhere classified

Interventions

Intervention 1: control group: the patients who receive general anesthesia. Intervention 2: epidural group: the patients who receive epidural anesthesia.
Treatment - Drugs
control group: the patients who receive general anesthesia
epidural group: the patients who receive epidural anesthesia

Sponsors

Vice Chancellor for Research, Mashhad University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: ASA I, II; laparoscopic cholecystectomy Exclusion criteria: patient,s refusal; coagulopathy; ischemic heart disease; heart failure; addiction; motion sickness; previous postoperative naseau and vomiting; increasing of surgery time due to adhesion

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood pressure. Timepoint: before of anesthesia and 15 minutes to end of surgery. Method of measurement: monitoring.;Heart rate. Timepoint: before of anesthesia and 15 minutes to end of surgery. Method of measurement: monitoring.

Secondary

MeasureTime frame
Naseau. Timepoint: postoperation to 24 hours later. Method of measurement: observation and question.;Vomiting. Timepoint: postoperation to 24 hours later. Method of measurement: observation and question.;Abdominal pain. Timepoint: recovery room to 24 hours later. Method of measurement: verbal analogue scale.;Shoulder pain. Timepoint: recovery room to 24 hours later. Method of measurement: verbal analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehryar Taghavi Gilani

Mashhad University of Medical Sciences

taghavim@mums.ac.ir+98 51 1852 5209

Outcome results

None listed

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