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Effect of 3 methods of general anesthesia and spinal anesthesia with and without lidocaine on pain after women laparoscopic surgeries

Effect of general anesthesia and spinal anesthesia with and without lidocaine on pain level following gynecologic laparoscopic surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016022226698N1
Enrollment
76
Registered
2016-03-23
Start date
2016-04-19
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

non inflematory disease of women genital. Diseases of the genitourinary system (N00-N99) Noninflammatory disorders of female genital tract

Interventions

Intervention 1: Intervention in first control group: Spinal anesthesia is done by 20 mg Bupivacaine 0/5% and then about 15 minutes after spinal anesthesia, the surgery begins. Before any painful stimu
Prevention
Intervention in first control group: Spinal anesthesia is done by 20 mg Bupivacaine 0/5% and then about 15 minutes after spinal anesthesia, the surgery begins. Before any painful stimuli a rectal dic
The second intervention group: Spinal anesthesia is done by 20 mg bupivacaine 0/5%.
Intervention in control group: general anesthesia

Sponsors

Tehran University of Medical Sciences , Deputy of Research
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 15-45; women in class of 1&2ASA who need laparoscopic surgery for assessing infertility and ectopioc pregnancy Exclusion criteria: contraindications of spinal, history of abdominal surgery; history of psychological diseases and anxiety; BMI> 35

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain after surgery. Timepoint: o, 2, 4, 6 and 12 hours after surgery and in discharge. Method of measurement: Visual analog scale.;Satisfaction of anesthesia method. Timepoint: after discharge. Method of measurement: numbered scale from 0- 10.

Secondary

MeasureTime frame
Headache. Timepoint: After surgery till discharge. Method of measurement: Questioneer.;Vomiting and nausea amount. Timepoint: After surgery till discharge. Method of measurement: questioneer.;The amount of opiod and analgesic drug administration. Timepoint: After surgery till discharge. Method of measurement: Check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahroo Rezaeinejad

Arash Women 's Hospital , Tehran University of Medical Sciences

mahroo_r@yahoo.com+98 21 7771 9922

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 27, 2026