Clinical study on the treatment of postpartum sacroiliac joint dislocation by osteopathy and soft tissue release

Phase 1

Recruiting

• Conditions: Sacroiliac Joint Disorder

• Registration Number: ITMCTR2024000036
• Lead Sponsor: The Second Affiliated Hospital of Yunnan University of Traditional Chinese Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

1. Postpartum female patients aged between 18 and 45 years;
2. Patients with anteroposteric dislocation who meet the above diagnostic criteria for postpartum SJD;
3. Postpartum related laboratory examination results showed no obvious abnormalities, excluding other factors;
4. The patient's communication ability and educational level can communicate with the researchers normally;
5.Women after 6 weeks of delivery (about 42 days) [22];
6. Voluntary subjects (patients) sign informed consent (see Appendix 1)

Exclusion Criteria

1. Non-postpartum female patients;
2.persons under the age of 18 and over the age of 45;
3.Those who do not meet the diagnostic criteria for postpartum SJD;
4.Patients with cardiovascular and cerebrovascular diseases, liver diseases, kidney diseases and other serious primary diseases, osteoporosis, bone hyperplasia and mental illness;
5. Eclampsia, amniotic fluid embolism, acute premature rupture of membranes, fetal distress, uterine rupture and other serious obstetric complications, serious injury of pubic symphysis, urinary tract infection, etc.
6. Pelvic fracture, congenital developmental deformity of pelvis, tuberculosis of lumbar spine, ankylosing spondylitis, spinal cord tumor, lumbar spondylolisthesis, lumbar disc herniation, etc.;
7. Patients within half a year after caesarean section;
8. Unable to cooperate with the completion of medical record data collection;
9.In the course of treatment, there are serious co-morbidity or deterioration of the condition.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
VAS;M-JOA;