Status:
COMPLETED
Hysterectomy - A Regional Intervention Study
Lead Sponsor:
University Hospital, Linkoeping
Conditions:
Benign Hysterectomy
Postoperative Recovery
Eligibility:
FEMALE
18-55 years
Phase:
NA
Brief Summary
Approximately 4,000 procedures with hysterectomy for benign indication are performed annually in Sweden. There are large differences in preoperative information, planning of surgery and surgical techn...
Detailed Description
Background Approximately 4,000 procedures with hysterectomy for benign indication are performed annually in Sweden. There are large differences between clinics in Sweden in the proportion of hysterect...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Women 18 - 55 years old.
- Women undergoing hysterectomy for benign indication.
- Women with ASA 1 - 3.
- Women who understand and can express themselves in Swedish.
- Women who, by signing "Informed Consent", agree to participate in the study after written and oral information.
- Women who participate and respond to the surveys in the GynOp register.
- Women who have access to an I-phone, smartphone, computer or tablet and who can use the study-specific mobile application. (Does not apply to sub-study 1).
- Exclusion criteria
- Women where both ovaries are removed during the operation.
- Women undergoing hysterectomy for prolapse indication.
- Women undergoing hysterectomy for cancer prophylactic indication.
- Women undergoing hysterectomy for gender reassignment purposes.
- Women with intellectual disabilities to such an extent that they can not fill in the relevant questionnaires etc. or if they do not understand the meaning of participating in the study or where there may be ethical doubts about the patient's participation in the study.
- Women who have a mental illness of such severity that the doctor in charge considers it inappropriate for the patient to be included in the study.
Exclusion
Key Trial Info
Start Date :
September 4 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2024
Estimated Enrollment :
230 Patients enrolled
Trial Details
Trial ID
NCT05255120
Start Date
September 4 2020
End Date
October 1 2024
Last Update
December 16 2024
Active Locations (2)
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1
University Hospital
Linköping, Sweden, 58185
2
Vrinnevisjukhuset
Norrköping, Sweden, 58185