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Comparison of inhalation anesthesia by isoflurane and intravenous anesthesia by propofol for laparoscopic cholecystectomy surgery

Comparison of inhalation anesthesia by isoflurane and intravenous anesthesia by propofol for laparoscopic cholecystectomy surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014080715795N1
Enrollment
60
Registered
2015-01-23
Start date
2014-05-22
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

Inhaled anaesthetics. Inhaled anaesthetics

Interventions

Intervention 1: 7ml/kg normal saline with Isofluran 1.5%. Intervention 2: 7ml/kg normal saline with Propofol 100µg/kg/min.
Treatment - Drugs
7ml/kg normal saline with Isofluran 1.5%
7ml/kg normal saline with Propofol 100µg/kg/min

Sponsors

Ardabil University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: laparoscopic cholecystectom; aged 15-80 years; ASA class I and II Exclusion criteria of the study: drug allergy; drug addiction; common cold; heart disease, kidney disease and hypertension; patient dissatisfaction; sedative drugs

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of discharge from recovery. Timepoint: After entering recovery. Method of measurement: Obtain recovery discharge criteria.

Secondary

MeasureTime frame
Blood pressure. Timepoint: Every 5 min during anesthesia. Method of measurement: Pressure gauge.;Heart rate. Timepoint: Every 5 min during anesthesia. Method of measurement: ECG monitor.;Time of Awakening. Timepoint: After discontinuation of anesthetic drugs. Method of measurement: Obey orders.;Hoarseness. Timepoint: In the first 24 hours after surgery. Method of measurement: According to the patient and their relatives.;Nausea and vomiting. Timepoint: In the first 24 hours after surgery. Method of measurement: According to the patient and carers.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Masood Entezariasl

Ardabil University of Medical Sciences

m.entezari@arums.ac.ir+98 45 3325 1688

Outcome results

None listed

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