Urological and Genital Diseases: Stress incontinence Urological and Genital Diseases
Conditions
Interventions
Each volunteer will be studied for the duration of the operation, until completion of the post-operative questionnaire and urodynamic studies, 3 h postoperatively. The average length of the procedure
Sponsors
Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Patients will be recruited from the clinical gynaelogical practice of Mr P Toozs-Hobson and Mr Emens. Individuals scheduled for suburethral sling surgery will be invited to participate in the investigation. Written consent will be obtained in all cases. We aim to recruit 25 patients to each arm of the study. Inclusion criteria: first operative procedure for stress incontinence.
Exclusion criteria
Exclusion criteria: 1. Contradiction to spinal anaesthesia 2. Unable/unwilling to give consent 3. Significant respiratory/cardiovascular disease/epilepsy 4. Allergy to propofol, opioids and local anaesthetics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Outcomes will be assessed by indices of patient satisfaction, satisfaction for surgical conditions, perioperative sedation scores, oxygenation, haemodynamic variables and the impact of anaesthetic technique on return of bladder sensation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed