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Total Versus Subtotal Abdominal Hysterectomy

Randomized Clinical Trial of Total Versus Subtotal Abdominal Hysterectomy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01880710
Enrollment
319
Registered
2013-06-19
Start date
2012-08-31
Completion date
2014-02-28
Last updated
2014-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign Uterine Disease

Keywords

long term follow-up, urinary incontinence, pelvic organ prolapse, total versus subtotal hysterectomy

Brief summary

319 Women undergoing hysterectomy for benign (not cancer) indications were randomly allocated to 2 types of surgery (Total (TAH) and Subtotal (SAH)) abdominal hysterectomy 15 years ago. They were followed by questionnaire at time of surgery and up to 5 years (not yet published) after the surgery and evaluated regarding following outcomes: Urinary incontinence, pain, bowel problems, per and postoperative complications, sexuality, quality of life, pelvic organ prolapse and vaginal bleeding. Now the investigators are conducting a 15 year follow up with the same out-come measures but also including physical examinations regarding Urinary incontinence, voiding difficulties, pelvic organ prolapse and problems with the cervix. The investigators' hypothesis is that several of the out-come measures will be present in more cases than earlier due to age and menopausal changes. The investigators expect more urinary incontinence in the subtotal group as this was seen at earlier follow ups. The investigators expect to find more women with pelvic organ prolapse with the physical examination than by questionnaire alone, possibly with a higher incidence in the subtotal group.

Detailed description

The study included women who were offered a hysterectomy for benign uterine disease such as: metrorrhagia, menorrhagia, fibroids, endometriosis,and pelvic pain. Women in need of hysterectomy for malignant disease or because of prolapse of the uterus were not included. They were followed up by a questionnaire covering all outcome measures as described above. Background information was registered in a second questionnaire prior to surgery. All gynaecological departments in Denmark were invited to join the trial. 11 departments contributed randomized patients to the trial. the results up to 1 year after surgery have been published, links can be found in the citation list. The results from the 5 year follow up have not yet been published. The questionnaire used in this trial consists of the validated SF-36 (Short Form 36) quality of life questionnaire as well as a thorough questionnaire regarding the outcome measures described elsewhere. The entire questionnaire was validated prior to the beginning of the trial. A second questionnaire has been added in the 15 year follow up: PFDI-20(Pelvic Floor Distress Inventory 20). The investigators included this, as it is more thorough regarding pelvic organ prolapse and in particular a bother measure than the original questionnaire. The 20 min. pad-weighing test has been tested against the 1 hour gold-standard used by the ICS (International Continence Society) and has been found to give comparable results.

Interventions

Subtotal abdominal hysterectomy where the body of the uterus is removed but the cervix is spared.

total abdominal hysterectomy where the body as well as the cervix of the uterus are removed.

Sponsors

University of Southern Denmark
CollaboratorOTHER
Zealand University Hospital
CollaboratorOTHER
Rigshospitalet, Denmark
CollaboratorOTHER
Nykøbing Falster County Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

-Women undergoing abdominal hysterectomy for benign uterine disease at a gynaecological department in Denmark (15 years ago)

Exclusion criteria

* malignant disease * mental disease * diabetes * neurological disease * not able to read and write Danish * pelvic organ prolapse as the reason for hysterectomy * prior surgery for urinary incontinence

Design outcomes

Primary

MeasureTime frameDescription
change in Urinary incontinence from baseline (preoperatively)2 months, 6months, 1, 5 and 15 years postoperativelyurinary incontinence measured by questionnaire filled out by the participants at each time point as well as a more objective measure: pad weighing test and voiding diary at 15 years

Secondary

MeasureTime frameDescription
pelvic organ prolapsepreoperatively, 2 months, 6months, 1, 5 and 15 years postoperativelysubjective measure by questionnaire at each time point as well as objective measure by POP-Q measurement at 15 years
cervical problems in the SAH grouppreoperatively, 2 months, 6months, 1, 5 and 15 years postoperativelyquestionnaire regarding bleeding at each time point, pap-smear regarding dysplasia at 15 years discharge summaries from hospital admissions/contacts regarding cervical problems.
voiding difficulties and LUTS (Lower Urinary Tract Symptoms)preoperatively, 2 months, 6 months, 1, 5 and 15 years postoperativelycovered by the questionnaire at each time point regarding urinary tract infections and problems emptying the bladder. In addition the 15 year follow up consists of uroflow, dip-stick for urinary infection as well as post-voiding ultrasound of the bladder to detect urinary retention.

Other

MeasureTime frameDescription
quality of lifepreoperatively, 2 months, 6months, 1 and 15 years postoperativelySF-36 questionnaire at each time point
per- and postoperative complicationspreoperatively, 2 months, 6months, 1, 5 and 15 years postoperativelyquestionnaire at each time points and case records regarding related surgery (hernia, bowel obstruction, removal of the cervix, surgery for urinary incontinence and pelvic organ prolapse)looked up in the clinical registry
sexualitypreoperatively, 2 months, 6months, 1, 5 and 15 years postoperativelyquestionnaire at each time point
pelvic painpreoperatively, 2 months, 6months, 1, 5 and 15 years postoperativelyquestionnaire at each time point
bowel problemspreoperatively, 2 months, 6months, 1, 5 and 15 years postoperativelyquestionnaire at each time point

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 16, 2026