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Laparoscopic Hysterectomy - Outpatient Versus Inpatient Regimen (LH)

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University of Aarhus

Status

Completed

Conditions

Outpatient Hysterectomy

Treatments

Procedure: Total laparoscopic hysterectomy

Study type

Interventional

Funder types

Other

Identifiers

NCT02933047
1-16-02-212-13 (Other Identifier)
5711674

Details and patient eligibility

About

Laparoscopic Hysterectomy (LH) is increasingly used as a standard surgical approach to hysterectomy. It is a safe procedure with low rates of complications and readmissions. Increasing evidence indicates that LH may be suitable for an outpatient setting but this may impair patient's satisfaction in more than 25% of cases. In addition, change from in-patient care to day case surgery might influence readmission rates and postoperative physical activity. No data are available on the current length of sick leave in Danish patients after hysterectomy, and the effects of outpatient surgery on this parameter are difficult to predict. A randomized controlled trial of LH performed as an outpatient procedure compared with today's inpatient standard will provide a firm platform for future planning of routine treatment of patients with need of hysterectomy for benign indications.

Full description

Hysterectomy is the most frequent gynecological operation world wide and the indication is often benign. The women are healthy and young with a median age below 50 years. In Denmark, hysterectomy is performed as an inpatient procedure with a median hospitalization of 1 day. Hysterectomies in Denmark are distributed by 45% abdominal hysterectomies (AH), 35% vaginal hysterectomies (VH) and 20% laparoscopic hysterectomies (LH). There is no final consensus whether VH or LH should be recommended as first choice but LH is gaining more and more acceptance. Increasing evidence indicates that LH may be suitable for an outpatient setting. Data seem to assure that outpatient LH is feasible but patient's satisfaction in this setting remains an open question. A detailed analysis of data from a Norwegian study indicates that patients reporting dissatisfaction with the early discharge amounts to 25-38%. Such a decrease in patient's satisfaction would present a significant problem, and a randomized controlled study of sufficient size with focus on this aspect is therefore needed.

Recommendations on postoperative sick leave vary considerably, due to lack of evidence-based guidelines and no firm data are available on the relation between outpatient treatment and sick leave in gynecology.

This randomized controlled study attempt to examine outpatient LH and patient satisfaction and related subject as readmissions and complications, time to return to work, physical activity in the recuperation period and an overall socioeconomic calculation of the costs of LH in an in- and outpatient setting.

Enrollment

204 patients

Sex

Female

Ages

18 to 56 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Premenopausal women below 56 years who is in need of a hysterectomy for benign conditions.
  • Additional surgery is allowed in the gynecological area.
  • BMI and working status is NOT exclusion criteria's.

Exclusion criteria

  • Unable to read and write Danish to answer questionnaires.
  • Unable to walk to carry a pedometer.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

204 participants in 2 patient groups, including a placebo group

Outpatient LH
Active Comparator group
Description:
Patients in the intervention group are discharged within 6 to 8 hours after total laparoscopic hysterectomy.
Treatment:
Procedure: Total laparoscopic hysterectomy
Procedure: Total laparoscopic hysterectomy
Inpatient LH
Placebo Comparator group
Description:
Patients in the control group follow regular hospitalization and are discharged within 24 hours after total laparoscopic hysterectomy.
Treatment:
Procedure: Total laparoscopic hysterectomy
Procedure: Total laparoscopic hysterectomy

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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