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NCT06034106: Pomegranate
The Effect of Pomegranate (Punica Granatum L.) Peel Compress Application on Pain and Physical Function Status
NA trial testing Pomegranate (Punica granatum) peel compress in Pomegranate (P. Granatum) Peel Compress in 67 participants. Status unknown.
30 September 2023
Quick facts
| Lead sponsor | TC Erciyes University |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | supportive care |
| Enrollment | 67 |
| Start date | 14 April 2023 |
| Primary completion | 30 September 2023 |
| Estimated completion | 15 October 2023 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Pomegranate (Punica granatum) peel compress
- Hot compress
Conditions studied
- Pomegranate (P. Granatum) Peel Compress — all drugs for Pomegranate (P. Granatum) Peel Compress →
Sponsor
TC Erciyes University
Who can join
45 and older, any sex, with Pomegranate (P. Granatum) Peel Compress. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Osteoarthritis is the most common type of arthritis among rheumatologic diseases. Complementary therapies are one of the effective methods for pain control. This study was planned as a randomized controlled experimental study. For this purpose, patients diagnosed with knee osteoarthritis who applied to the Orthopedics Outpatient Clinic will be included. It was calculated that the study would include at least 67 patients. The study will be collected using patient information form, descriptive characteristics form, Visual Analog Scale (VAS) and WOMAC osteoarthritis application scale. It was planned as a randomized controlled experimental study to evaluate the effect of pomegranate peel (P. granatum) compress application on pain and function status. The study was divided into 3 groups as Pomegranate (Punica granatum) peel compress, hot compress and control group. Pomegranate (Punica granatum) peel compress was applied 3 days a week for 3 weeks by turning the powder into porridge check.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06034106 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by TC Erciyes University
- Last refreshed: 13 September 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06034106.
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