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The effectiveness of PRP Gel in wound healing caused by resection of Pilonidal sinus

Comparative study on potential of platelet-rich plasma Gel and regular dressing in duration of wound healing in patients who underwent pilonidal sinus surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016020418842N11
Enrollment
123
Registered
2016-03-16
Start date
2012-09-22
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

Pilonidal Sinus Disease with abscess. Pilonidal sinus with abscess

Interventions

Intervention 1: In intervention group,the obtained PRP was additionally injected into the depth (13mm) of the wound. It was also applied to center of each circle (0.1cc) and wound site (1 cm in diamet
Treatment - Drugs
In intervention group,the obtained PRP was additionally injected into the depth (13mm) of the wound. It was also applied to center of each circle (0.1cc) and wound site (1 cm in diameter) through inje
Classical dressing (sterile absorbent cotton gauze) was applied for the control group. Washing the wound with normal saline (0.9%) twice a day was ordered. Wound debridement was also done in order to

Sponsors

Vice chancellor for research,Tehran University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 47 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Any patient diagnosed with pilonidal sinus disease with a scheduled surgery. Exclusion criteria: lower platelet count of <103/µL; hemoglobin <10 mg/dl; anti-proliferative therapies such as chemotherapy and also radiation in past 3 months; anti-inflammation medications in past 2 weeks; growth factor therapies in last 2 weeks, history of diabetes, history of mal-absorption (celiac disease); any contra-indication in peripheral venues access ; not willing to participate in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Wound healing time. Timepoint: Weekly up to full healing. Method of measurement: Wound volume measurement by filling the wound with saline. The volume dispensed from the syringe equals the wound volume.;Quality of life. Timepoint: Weekly after start treatment up to average 8 weeks. Method of measurement: Quality of life questionnaire SF12 and 26.

Secondary

MeasureTime frame
Angiogenesis. Timepoint: In PRP group: between 4-6 weeks In control group: between 8-10 weeks. Method of measurement: Immuno Histochemistery (IHC) on biopsy sample.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKamran Alimoghadam

Hematology, Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sci

alimgh@sina.tums.ac.ir+98 21 8490 2635

Outcome results

None listed

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