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compairing the effects of neuroaxial and general anesthesia on postoperative quality of recovery after abdominal hysterectomy.

The effect of Spinal Anesthesia vs. General Anesthesia on analgesia& postoperative quality of recovery after abdominal hysterectomy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201309306148N3
Enrollment
100
Registered
2013-10-23
Start date
2013-09-01
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

Post operative analgesia after total abdominal hysterectomy. Acquired absence of uterus

Interventions

Intervention 1: Intervention group: 17.5 mg 0.5% bupivacaine with fentanyl 25 microgram was injected into subarachnoid space. Intervention 2: Control group: General anesthesia was induced with 0.1 mg/
Treatment - Drugs
Intervention group: 17.5 mg 0.5% bupivacaine with fentanyl 25 microgram was injected into subarachnoid space.
Control group: General anesthesia was induced with 0.1 mg/kg morphine and fentanyl 1-2 micrograms/kg and propofol 2 mg/kg, and atracurium 0.5 mg/kg. Continue of anesthesia will be with isoflurane 1-1

Sponsors

Vice-chancellor Of Research Babol University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: ASA physical status I and II females undergoing total abdominal hysterectomy for benign (noncancerous) disease. Exclusion criteria: Patients with a history of coagulopathy; recent infectioncurrent; use of an opioid analgesic or corticosteroid; history of migraine headache; gross neurologic impairment; suspected difficult airway

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Analgesia. Timepoint: 6, 24, 48 hour after surgery. Method of measurement: Visual analogues Scale.;Quality of recovery. Timepoint: 24, 48 hour after surgery. Method of measurement: QOR-40 questionnaire.

Secondary

MeasureTime frame
Heart Rate. Timepoint: Before induction, during surgery and after surgery. Method of measurement: ECG.;Blood Pressure. Timepoint: Before induction of anesthesia, during surgery and after surgery. Method of measurement: Non invasive BP Cuff.;Nausea & Vomiting. Timepoint: After Surgery. Method of measurement: Question & Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Hakimeh Alereza Amiri

Babol University Of Medical Sciences

halereza@yahoo.com; ans_dep@yahoo.com+98 11 1223 8296

Outcome results

None listed

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