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Comparsion of Coccydynia treatment with intractal manipulation concomitant to methyl prednisolone acetate injection & manipulation.

Comparsion of Coccydynia treatment with intractal manipulation concomitant to methyl prednisolone acetate injection & manipulation.

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT138811203317N1
Enrollment
30
Registered
2010-04-03
Start date
2009-03-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coccydynia. Sacrococcygeal Disorders not elsewhere classified Coccygodynia

Interventions

Intervention 1: Coccygeal Manipulation concomitant with methyl prednisolone acetate injection (40mg). Intervention 2: Three sessions of coccygeal manipulation.
Treatment - Drugs
Coccygeal Manipulation concomitant with methyl prednisolone acetate injection (40mg)
Three sessions of coccygeal manipulation

Sponsors

Shiraz University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Presence of chronic (>2 months) Coccydynia, age between 18 and 70, no prior other treatments, consent to the study. Exclusion criteria: Presence of acute fracture of coccyx, Presence of osteoporosis, diabetes, or rheumatologic Disorders, known malignancy or congenital malformations.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Coccydynia treatment. Timepoint: One day, One week, One month & three months after the procedure. Method of measurement: Using a VAS and paris (functional Coccydinia impact) questionnaires.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammadjavad Hadianfard

Shiraz University of Medical Sciences and Health Services

?hadianj@sums.ac.ir+98 71 1230 0040

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026