Comparing two treatments for tailbone pain
Official title: Comparative Effects of Levator Ani Release and Post Isometric Relaxation on Pain, Disability, and Quality of Life Among Patients With Coccydynia
Run by Riphah International University · NCT06109077 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing whether two different treatment methods can help people with tailbone pain feel better and improve their daily life.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 20 Years to 40 Years |
| Sex | All |
| Enrollment | 46 (estimated) |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Lahore, Punjab) |
| Trial ID | NCT06109077 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals aged 20-40 years who are drivers, office workers, or computer users experiencing tailbone pain.
✕Probably not a fit
Patients with neurological disorders, bone deficits, vascular abnormalities, rheumatoid arthritis, ankylosing spondylitis, fractures, or tumors may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to compare the effects of levator ani release exercises and post isometric relaxation techniques on pain, disability, and quality of life in patients suffering from coccydynia. A randomized control trial will be conducted at Jinnah Hospital in Lahore, involving 46 participants who will be randomly assigned to one of two treatment groups. The effectiveness of each intervention will be assessed using a pain and disability questionnaire at the start and after four weeks of treatment. Data analysis will be performed using SPSS software to determine the outcomes of each treatment method.
Why it matters
Potential benefit: If successful, this study could provide effective non-surgical treatment options for patients suffering from coccydynia.
How similar studies have gone: While there is limited data on the specific interventions being compared, similar studies have shown promise in treating coccydynia with physical therapy techniques.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria:• * Both gender * Age between 20-40 years * Drivers * Office workers * Computer users * Both gender * Age between 20-40 years * Drivers * Office workers * Computer users Exclusion Criteria: * Neurological disorders, * Bone deficits, * Vascular abnormalities, * Rheumatoid arthritis * Ankylosing spondylitis * Fracture * Tumor
Where it's running
-
Ittefaq
Lahore, Punjab, Pakistan Recruiting
Study contacts
- Principal investigator: Humera Mubashar, Ms — Riphah International University
- Study coordinator: Imran Amjad, Phd
- Email: imran.amjad@riphah.edu.pk
- Phone: 03324390125
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Shock Wave Therapy vs High-Intensity Laser Therapy for Tailbone Pain
This study tests whether shock wave therapy or high-intensity laser therapy reduces pain while sitting for adults with chronic tailbone pain.
-
Ultrasound-guided dextrose prolotherapy for coccyx pain
This will test whether ultrasound-guided 15% dextrose injections can reduce pain and improve function in adults (18–75) with chronic coccydynia not helped by conservative treatments.
-
Dextrose prolotherapy for chronic tailbone (coccydynia) pain
This study will try dextrose prolotherapy injections to see if they reduce chronic tailbone pain in adults who haven't improved after six months of conservative treatment.
-
Comparing two pain relief techniques for tailbone pain
This study is testing two different pain relief methods for people with chronic tailbone pain to see which one helps them feel better.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.