CClinicalTrials.gg
Status unknownNCT00181311Updated Oct 26, 2006

Investigation of the Incidence of Complications After Vaginal and Abdominal Hysterectomy

An observational study in Hysterectomy, sponsored by Maasland Hospital. Status unknown at 1 site in Netherlands. Open to female participants. Per ClinicalTrials.gov, last updated 2006-10-26.

Sponsored by Maasland Hospital · Observational

The sponsor has not verified this record recently (last verified Aug 2005), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Defined population
Time perspective
Other
Enrollment
200
Sex
Female
01

Study summary

The purpose of this study is to evaluate the short and long term complications after an abdominal or vaginal hysterectomy and to detect the prevalence of occult/subclinical haematomas and vaginal cuff abscesses and the postoperative course of these.

The investigators will also evaluate the physical and mental well being after a hysterectomy with a questionnaire and correlate these results with the occurrence of complications.

Read the detailed description

Hysterectomy is the most common major gynaecological operation performed worldwide.

The overall average rate of hysterectomy in the United States is 5.6 per 1000 women. There are three different procedures to perform a hysterectomy. The surgery can be approached abdominally, vaginally or as a laparoscopically assisted hysterectomy.

This study will contribute to the improvement of knowledge in short and long term complications and especially the prevalence of occult and subclinical haematomas and vaginal abscesses after abdominal or vaginal hysterectomy. The occurrence of short and long term complications will have an influence on the general well being of the patient. We will also evaluate the physical and mental well being of the patient after a hysterectomy.

After statistical analysis of the study outcome parameters, some conclusions can be drawn for the treatment policy after an abdominal or vaginal hysterectomy to reduce the complication rate and improve the general well being of our patients.

02

Conditions studied

  • Hysterectomy

Keywords

  • vaginal hysterectomy
  • abdominal hysterectomy
  • complications
  • physical well being
  • mental well being
03

In context

Lead sponsor

This is the only study on the registry with Maasland Hospital as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Benign indication for undergoing of a hysterectomy
  • Written informed consent of the patient

Exclusion criteria

Exclusion Criteria:

  • Inability to undergo an operation due to high surgical or anaesthetic risk
  • Malignancy as indication for the hysterectomy
  • Patients with an enterocele or rectocele and who need prolapse surgery
05

Study design

Observational model
Defined population
Time perspective
Other
Enrollment
200 participants

Interventions

  • Procedurehysterectomy
06

Study locations

1 of 1 sites recruiting
  • Maasland Hospital
    Sittard, Limburg 6130 MB, Netherlands
    • Erik Jan Sollie, MD · Contact · +31(0)464597787
    • Martine Wassen · Principal investigator
    Recruiting
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 26, 2006, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00181311
Lead sponsor
Maasland Hospital
First posted
Sep 16, 2005
Start date
Aug 2005
Completion
Oct 2006
Last update
Oct 26, 2006

Study contacts

Erik Jan Sollie, MD
Contact
e.sollie@orbisconcern.nl
+31(0)464597787
Erik Jan Sollie, MD
study chair · Maasland Hospital
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2005. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion