Combined Anesthesia for Laparoscopy Surgery in Gynecology

Rambam Health Care Campus

Status: Unknown

Conditions: Pain

Treatments: Procedure: Spinal anesthesia with Fentanyl+ Morphine

Study type: Interventional

Funder types: Other

Identifiers

NCT01246323

COBINED ANASTHESIA GYNECOLOGY

Details and patient eligibility

About

The purpose of this study is to determine whether combined anesthesia will provide better pain control for the postoperative period following gynecological laparoscopy surgery.

Full description

Following signing an informed consent patients who are scheduled for gynecological laparoscopy surgery for benign disease will randomized to general vs. combined general and spinal anesthesia.

During the postoperative period data regarding pain level as evaluated by visual analogue scale (VAS), number of doses of pain relief drugs, satisfaction and number of day in hospitalization will be collected from patient charts.

Enrollment: 40 estimated patients

Sex: Female

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. American Society of Anesthesiology (ASA) physical status classification system:ASA I-III.
2. Benign Gynecological Laparoscopy surgery

Exclusion criteria

1. Patients who are not capable to sign the consent form.
2. Women with known allergy to the medication used in spinal analgesia.
3. Patients who are pregnant or lactating.
4. Patients with contraindication to spinal analgesia.
5. Patients who use opioid on a regular base.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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40 participants in 2 patient groups

combined anesthesia

Active Comparator group

Description:

Patients will receive spinal and general anesthesia for benign laparoscopy gynecological surgery

Treatment:

Procedure: Spinal anesthesia with Fentanyl+ Morphine

Control

No Intervention group