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Impact on Quality of Life of Osteopathic Visceral Mobilizations After Endometriosis Surgery (MOVENDOP)

U

University Hospital, Clermont-Ferrand

Status

Enrolling

Conditions

Osteopathy in Diseases Classified Elsewhere
Endometriosis

Treatments

Other: osteopatic visceral mobilization

Study type

Interventional

Funder types

Other

Identifiers

NCT06553989
2023-A02653-42 (Other Identifier)
RBHP 2023 BOURDEL

Details and patient eligibility

About

One of the most common post-operative complications of gynaecological surgery, and in particular endometriosis surgery, is the formation of peritoneal adhesions. After laparotomy, it affects up to 90% of patients. Minimally invasive techniques (such as laparoscopy) reduce the risk of adhesion formation, but cannot totally prevent it. Adhesions can lead to chronic pelvic pain, dyspareunia, digestive disorders and infertility. Various strategies and devices have been developed to try and limit adhesion formation, but their effectiveness has not been fully proven in the literature. The only real treatment for adhesions is adhesiolysis, although adhesions often reform. The quality of surgery remains the best means of preventing adhesion formation. To reduce the morbidity associated with pelvic adhesions, it is essential to develop alternative, non-invasive, anti-adhesive methods such as manual osteopathic visceral mobilization.

Enrollment

63 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Woman of legal age
  • Indication for surgery for infiltrating endometriosis
  • Able to give informed consent to participate in research
  • Patient included in NO ENDO (national endometriosis observatory promoted by Clermont-Ferrand University Hospital)

Exclusion criteria

  • Indication for surgery for superficial endometriosis
  • Patient of legal age, under guardianship or trusteeship
  • Pregnant or breast-feeding patient
  • Patients not affiliated to the social security system
  • Patients who do not speak French
  • Patients under court protection
  • Simultaneous participation in another study
  • Refusal to participate.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

63 participants in 2 patient groups

Control group
No Intervention group
Description:
patients operated for endometriosis without osteopathic visceral mobilization
Experimental group
Experimental group
Description:
patients operated for endometriosis with osteopathic visceral mobilization
Treatment:
Other: osteopatic visceral mobilization

Trial contacts and locations

1

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Central trial contact

Lise Laclautre

Data sourced from clinicaltrials.gov

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