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OpenTrials
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NCT Number: NCT07496814

Comparison of the Outcomes of Total Laparoscopic Hysterectomy Versus Total Abdominal Hysterectomy for Benign Gynecologic Conditions in a Limited-resources Setting.

Minimally invasive hysterectomy (laparoscopic) is associated with shorter hospital stay, less blood loss, faster recovery, and improved early postoperative quality of life compared with open abdominal hysterectomy. However, in low-resource settings, barriers such as equipment availability, cost, and limited surgeon experience may influence outcomes.

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Key information

Age range

35 year–65 year

Sex eligibility

Female

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women aged 35-65 years.
  • Indication for elective hysterectomy for benign disease.
  • Uterine size ≤ 16 weeks.

Exclusion criteria

  • Malignancy or suspicion of malignancy.
  • Prior extensive abdominal surgery with dense adhesions.
  • Morbid obesity, BMI more than 40
  • Severe cardiopulmonary disease.
  • Pregnancy.
  • Refusal participates in study

Treatment and study plan

Primary outcomes

  1. length of postoperative hospital stay

    Time frame: beseline

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Mar 27, 2026
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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.