Actively Recruiting
Vaginal NOTES Hysterectomy Versus Vaginal Hysterectomy
Led by Zuyderland Medisch Centrum · Updated on 2025-08-14
124
Participants Needed
2
Research Sites
234 weeks
Total Duration
On this page
Sponsors
Z
Zuyderland Medisch Centrum
Lead Sponsor
C
Catharina Ziekenhuis Eindhoven
Collaborating Sponsor
AI-Summary
What this Trial Is About
Rationale: Natural orifice transluminal endoscopic surgery (NOTES) is a minimal invasive technique using the natural body orifices like stomach, oesophagus, bladder, rectum and vagina to access the human body for surgery. In 2012, the first vaginal NOTES (vNOTES) hysterectomy was performed. Potential benefits of vNOTES hysterectomy, also called the vaginal assisted NOTES hysterectomy (VANH) are no visible scars, less pain and a shorter hospital stay compared with laparoscopic hysterectomy as shown in the HALON trial. Up to now, no studies have compared the vNOTES hysterectomy with vaginal hysterectomy. Objective: The aim of this study is to compare the vNOTES hysterectomy with the vaginal hysterectomy for same day-discharge (SDD), complications, treatment related outcomes, post-operative recovery, quality of life and cost-effectiveness. Study design: The study concerns a single-blinded, multicentre, randomised controlled trial. Study population: Eligible women who fulfill the inclusion criteria and will undergo a hysterectomy for benign indication. Intervention: The study population will be randomly allocated to the VANH-group, who undergo a vaginal assisted NOTES hysterectomy (intervention group) or the vaginal hysterectomy group (control-group) and the participants will be single blinded. The pre- and postoperative care will be the same for both groups. Main study parameters/endpoints: Primary outcome is the percentage of patients that underwent the hysterectomy as in SDD setting. A total of 41 patients should be included in the control group and a total of 83 patients in the intervention group, using an enrollment ratio of 1:2, with an alpha of 0.05 and a power of 0.8. The secondary outcomes are complications, treatment related outcomes, post-operative recovery, quality of life and cost-effectiveness. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: vNOTES is a new surgical technique, but a combination of two existing techniques namely the vaginal hysterectomy and the laparoscopic hysterectomy. Only one randomized controlled trial has been published, comparing the total laparoscopic hysterectomy (TLH) with the VANH, which shows no inferiority of the vNOTES technique compared to a laparoscopy. A recent case series study has been published about the complication rate in VANH. There was a total complication rate in the hysterectomy group of 5.2%, in which 1.4% was intra-operative and 3.8% postoperative. Theoretically it is possible that the VANH causes less intra-operative complications because of an improved view during the procedure. No further literature is known about VH versus VANH. Participants of the study should fill in multiple questionnaires before randomization and postoperative about their general health, pain experience and used analgesics.
CONDITIONS
Official Title
Vaginal NOTES Hysterectomy Versus Vaginal Hysterectomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Written and orally given informed consent
- 18 years and older
- Native Dutch speaker or fluent in Dutch speaking and writing
- Medical indication for hysterectomy due to benign condition
- Vaginal hysterectomy possible as judged by experienced gynecologist
You will not qualify if you...
- Contraindications for vaginal hysterectomy such as large uterus or insufficient descent
- History of more than one cesarean section
- History of endometriosis
- History of rectal surgery
- History of pelvic radiation
- Suspected rectovaginal endometriosis
- History of pelvic inflammatory disease or suspected adhesions
- Virginity
- Current pregnancy
- Need for anterior or posterior colporrhaphy during same surgery
- Need for mid urethral sling procedure
- Uterus myomatosus if judged not removable vaginally by surgeon
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Catharina Medical Centre
Eindhoven, North Brabant, Netherlands
Not Yet Recruiting
2
Zuyderland Medical Centre
Heerlen, North Brabant, Netherlands, 5644AD
Actively Recruiting
Research Team
I
Ilse Bekkers
CONTACT
M
Martine Wassen
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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