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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04822428
Other study ID # SH2021
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 20, 2020
Est. completion date March 12, 2021

Study information

Verified date March 2021
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Forty female patients with age ranging from 30-40 years old were suffering from low back pain due to visceral dysfunctions participated in this study. They were recruited from a private clinic. They were assigned into two groups equal in number; Group (A): included twenty patients who received osteopathic manipulative techniques, 1 session per week for 3 weeks, and Group (B): included twenty patients who received only analgesic drugs.


Description:

Twenty patients received osteopathic manipulative techniques including Suboccipital release technique, diaphragmatic release.,mesentery release and Colonic manipulation were applied to the study group according to the patients' needs. The treatment program comprised a total of 3 sessions for 3 weeks at one session per week for an average of 50 minutes per session. Twenty patients in the second group (control ) took only analgesics during the three weeks.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date March 12, 2021
Est. primary completion date March 12, 2021
Accepts healthy volunteers No
Gender All
Age group 30 Years to 40 Years
Eligibility Inclusion Criteria: - Non-specific low back pain for more than 12 weeks Exclusion Criteria: - Malignant tumor - Pregnancy - Acute ischemic bowel disease, - Intestinal obstruction, - surgery in the last six months

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Osteopathic manipulation
Osteopathic manipulative techniques including; suboccipital release technique,sacral release technique, diaphragmatic release, mesentery release, and Colonic manipulation

Locations

Country Name City State
Egypt Faculty of Physical Therapy Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The visual analog scale (VAS) The patient determined the pain intensity on a 10 cm scale marked with points ranging from predetermined no pain and excruciating pain change from baseline to after 3 weeks
Primary The Oswestry Disability Index (ODI) (ODI) consists of 10 items on the degree of severity to which back (or leg) trouble has affected the ability to manage in everyday life. change from baseline to after 3 weeks
Primary Modified Schober's test (MST) the participant stood erect while the lumbosacral junction was marked as indicated by the dimples of Venus. For measuring the MST, we put a mark 5 cm below and 10 cm above the junction. The participant was asked to bend forward as far as possible and the stretched distance of these two points was measured as the MST value. change from baseline to after 3 weeks
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