Abdominal keyhole surgery with spinal anesthesia

Not Applicable

Completed

• Conditions: Gynecological diseases in the pelvis; Urological and Genital Diseases

• Registration Number: ISRCTN56613886
• Lead Sponsor: ESTHER

Brief Summary

2024 Results article in https://pubmed.ncbi.nlm.nih.gov/38929854/ (added 28/08/2024)

Detailed Description

Not available

Study Timeline

• Study Completion: 2020-10-30
• Study Start: 2024-07-01
• Last Update Posted: 9 September 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 93

Inclusion Criteria

1. Women who will undergo laparoscopic surgery in the lower abdomen
2. Minimum follow up of 6 months

Exclusion Criteria

1. Contraindication for loco-regional anesthesia
2. Do not consent to complete the questionnaire

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Measured using a survey before, during and post surgery:<br>1. Comfort of the patient and the surgeon<br>2. Pain during the operation<br>3. Feasibility of performing the surgery<br>4. Questions about satisfaction (changes or symptoms pre-and post-operatively, time of recovery, satisfaction with information, improvement in well being, recommending the operation)

Secondary Outcome Measures

Name	Time	Method
Measured using self-report on a 0–10 scale (0=minimum, 10=maximum impairment) before, during and post surgery:<br>1. Symptoms (pain, postoperative symptoms)<br>2. Side effects (headache, nausea)<br>3. Quality of life (felt tired/drained/lacking energy, felt irritable/snappy, felt depressed/tearful, general evaluation of health, change in body perception)