Tubal Sterilization Clinical Trial
Official title:
Vaginal Natural Orifice Trans-luminal Endoscopic Surgery (vNOTES) Salpingectomy for Tubal Sterilization: Clinical Outcomes and Learning Curve Analysis: A Multicentre Prospective Study
The evolution from classical open surgery to laparoscopic surgery has led to a significant reduction of morbidity and mortality. Newer advances such as development of single port laparoscopic surgery and scarless Natural Orifice Transluminal Endoscopic Surgery (NOTES) have moved forward the practice in "Minimally Invasive Surgery". Recently, clinical application of vNOTES has broadened significantly in the field of gynaecological surgery. As the application of vNOTES is increasing, it is deemed mandatory to assess the clinical outcomes and the learning curve (LC) of this novel technique. There is a paucity of reports in the literature analysing prospectively the clinical outcomes the LC of vNOTES in the gynaecological field. To the investigator's knowledge, there is no published prospective multicentre study that aims to evaluate the peri- and postoperative outcomes and the LC of salpingectomy for tubal sterilization by the technique of vNOTES.
Status | Recruiting |
Enrollment | 240 |
Est. completion date | March 2024 |
Est. primary completion date | March 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: - 18 - 50 years - Non-prolapsed uterus - Asking for tubal sterilisation - Any parity - Written informed consent Exclusion Criteria: - History of pelvic inflammatory disease. - Recto-vaginal endometriosis. - Suspicion of genital tract malignancy. - Active lower genital tract infection. - History of rectal surgery. - Stage III or IV Uterine prolapse (defined by the International Continence Society classification). - Complete obliteration of the posterior douglas pouch determined by pelvic examination. - Virginity. - Failure to provide written informed consent. |
Country | Name | City | State |
---|---|---|---|
Belgium | CHU Brugmann | Brussels | |
Belgium | Clinique Saint-Jean | Brussels | |
Belgium | Cliniques Universitaires Saint LUC | Brussels | |
Belgium | CHU Liège - site CHR Liège | Liège |
Lead Sponsor | Collaborator |
---|---|
Jani Jacques |
Belgium,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of women successfully operated (salpingectomy) for tubal sterilization using vNOTES technique as a one day procedure. | The proportion of women who were successfully operated (salpingectomy) for tubal sterilization using vNOTES technique as a one day procedure will be measured as the primary outcome of effectiveness.
Successful salpingectomy for tubal sterilization using vNOTES technique as a one day procedure is defined by: Complete retrieval of fallopian tube(s) (pathological confirmation). No conversion into laparoscopy or open surgery. Discharge from hospital on day 0 post-operatively. |
2 years | |
Primary | Learning Curve Assessment. | The Assessment of the learning curve of salpingectomy by the technique of vNOTES in young and experienced surgeons is another primary outcome of our study. | 2 years | |
Secondary | Intraoperative or postoperative complications | Intraoperative or postoperative complications detected during the first 6 weeks of surgery and classified based on the Clavien-Dindo classification. | 6 weeks | |
Secondary | Postoperative pain scores | Postoperative pain scores measured using a visual analog scale twice a day from day 1 to 7. | 7 days | |
Secondary | Pain drugs intake | The total amount of pain drugs taken during the first week following surgery | 7 days | |
Secondary | Number of days of absence from work | Number of days of absence from work | 2 years | |
Secondary | Short Sexual Functioning Scale (SSFS) | Sexual well-being by self-reporting the Short Sexual Functioning Scale (SSFS). | baseline | |
Secondary | Short Sexual Functioning Scale (SSFS) | Sexual well-being by self-reporting the Short Sexual Functioning Scale (SSFS). | 3 months after baseline | |
Secondary | Short Sexual Functioning Scale (SSFS) | Sexual well-being by self-reporting the Short Sexual Functioning Scale (SSFS). | 6 months after baseline | |
Secondary | Pain on sexual intercourse | Occurrence and severity of pain on sexual intercourse self-reported by the patient by using a simple questionnaire. | baseline | |
Secondary | Pain on sexual intercourse | Occurrence and severity of pain on sexual intercourse self-reported by the patient by using a simple questionnaire. | 3 months after baseline | |
Secondary | Pain on sexual intercourse | Occurrence and severity of pain on sexual intercourse self-reported by the patient by using a simple questionnaire. | 6 months after baseline |
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