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The effect of aminophylline on the recovery time of hysterectomy patients under general anesthesia

Investigating the effect of aminophylline on the recovery time of hysterectomy patients under general anesthesia; A randomized double-blind clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170314033069N5
Enrollment
74
Registered
2022-12-31
Start date
2023-01-20
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Investigating the effect of aminophylline on the recovery time of patients after hysterectomy. Complications of anesthesia during labor and delivery

Interventions

Intervention 1: Intervention group: After uterus removal by the surgeon, patients in the intervention group will receive 3 milligrams per kilogram of intravenous aminophylline (manufactured by Caspian

Sponsors

Rasht University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists (ASA) I,II Candidate for hysterectomy under general anesthesia in Alzahra hospital Women aged 30 to 70

Exclusion criteria

Exclusion criteria: Hysterectomy due to malignancy Any history of allergy to aminophylline or drug components Any dysfunction of the liver, including liver cirrhosis, fatty liver, etc smokers People who have recently received or are taking cimetidine, ciprofloxacin, and macrolides such as erythromycin and clarithromycin History of any type of arrhythmia or neurological disorder such as epilepsy Patient dissatisfaction

Design outcomes

Primary

MeasureTime frame
Emergence from anesthesia. Timepoint: From the time of discontinuing administration of anesthetic drugs to the time of patient's eyes getting open after calling her/his name. Method of measurement: Time measurement.;Extubation time. Timepoint: From the time of discontinuing administration of anesthetic drugs to the time of removing the endotracheal tube. Method of measurement: Time measurement.;Recovery time. Timepoint: From the time of discontinuing administration of anesthetic drugs to the time of transferring the patient to the ward. Method of measurement: Time measurement.

Secondary

MeasureTime frame
Mean arterial blood pressure (MAP). Timepoint: Before administration of aminophylline and normal saline and then every 5 minutes until transferring to recovery, then every 15 minutes during recovery. Method of measurement: Blood pressure measurement with mercury sphygmomanometer.;Heart rate. Timepoint: Before administration of aminophylline and normal saline and then every 5 minutes until transferring to recovery, then every 15 minutes during recovery. Method of measurement: Heart rate monitor.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Gelareh Biazar

Rasht University of Medical Sciences

gelarehbiazar1386@gmail.com+98 13 3332 9524

Outcome results

None listed

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