Follow-up Strategies for Improved Postoperative Recovery After Benign Hysterectomy

NCT01526668 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 525

Last updated 2022-02-07

No results posted yet for this study

Summary

The purpose of the study is to investigate the effect of four different follow-up strategies on postoperative recovery following vaginal or abdominal hysterectomy for benign conditions. Furthermore the investigators aim to examine associations between preoperative thresholds for pain (thermal and pressure) and postoperative pain and development of chronic pelvic pain after benign hysterectomy.

Conditions

  • Hysterectomy
  • Genital Diseases, Female
  • Pain

Interventions

BEHAVIORAL

Follow-up strategy

Comparison of different follow-up strategies

BEHAVIORAL

No contact after discharge

Sponsors & Collaborators

  • University Hospital, Linkoeping

    lead OTHER

Principal Investigators

  • Preben Kjolhede, MD, PhD · Department of Obstetrics and Gynecology, University Hospital, 58185 Linkoping, Sweden

  • Ninnie Borendal Wodlin, MD, PhD · Department of Obstetrics and Gynecology, University Hospital, S-58185 Linkoping, Sweden

  • Lena Nilsson, MD, PhD · Department of Anesthesiology, University Hospital, S-58185 Linkoping, Sweden

  • Gunilla Sydsjo, PhD · Department of Obstetrics and Gynecology, University Hospital, S-58185 Linkoping, Sweden

  • Gulnara Kassymova, MD · Department of Obstetrics and Gynecology, University Hospital, S-58185 Linkoping, Sweden

  • Peter Lukas, MD · Department of Obstetrics and Gynecology, University Hospital, S-58185 Linkoping, Sweden

  • Björn Gerdle, MD, PhD · Pain and Rehabilitation Center, University Hospital, 581 85 Linkoping, Sweden

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-10-11
Primary Completion
2018-01-31
Completion
2018-01-31

Countries

  • Sweden

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01526668 on ClinicalTrials.gov