Total abdominal hysterectomy
ProcedureTotal abdominal hysterectomy
NCT Number: NCT00876057
The purpose of this study is to determine whether psychological well-being, recovery and sexuality differs in women undergoing subtotal and total abdominal hysterectomy.
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Female
Interventional
Phase 4
Höglandssjukhuset i Eksjö, Eksjö, Sweden
An additional study study based on the material in original study started in april 2011. The purpose of this study is to investigate the development of pelvis organ prolapse in the long term (median eleven years after hysterectomy and by questionnaires, Pelvic-floor Distress Inventory SF-20 analyze if patient reported symptoms regarding urinary-and bowels functions differs regarding the method of hysterectomy.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Total abdominal hysterectomy
Subtotal abdominal hysterectomy
Time frame: One year after surgery
Time frame: Five weeks after surgery
Time frame: One year
Time frame: 7-14 years
Follow-up median eleven years after the initial hysterectomy. Clinical investigation including POP-Q.
Time frame: 7-14 years
Follow-up median eleven years after the initial hysterectomy. Questionnaire (Pelvic Floor Dysfuntion Inventoy).
University Hospital, Linkoeping
Other
Subtotal Versus Total Abdominal Hysterectomy- a Prospective Randomised Comparison of Medical , Psychological and Sexual Effects.
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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