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A retrospective study on the effectiveness and safety of different fractionated doses of radiotherapy after keloid surgery

A retrospective study on the effectiveness and safety of different fractionated doses of radiotherapy after keloid surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129559
Enrollment
Unknown
Registered
2026-08-06
Start date
2026-08-10
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Keloids: Changes in the appearance and histology of normal skin tissue caused by various skin injuries. They appear raised above the normal skin surface, extend beyond the original injury area, and continue to grow, sometimes accompanied by itching or pain.

Interventions

Conventional fractionation group (4Gy×5):None
Large fractionation group (5Gy×4):None

Sponsors

China National Nuclear Corporation 416 Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age 18–80, any gender; 2.Clinically and pathologically confirmed keloids, with complete surgical removal; 3.Time from surgery to first radiotherapy <= 24 hours; 4.Radiotherapy using 6–9 MeV electron beams, total dose 20Gy; 5.Complete follow-up data, with last follow-up at least 12 months after surgery.

Exclusion criteria

Exclusion criteria: 1.Did not receive radiotherapy promptly after surgery; 2.Severe diabetes complications, autoimmune skin diseases, or history of malignant tumors; 3.Pregnant or breastfeeding women; 4.Keloid area has acute infection or poor wound healing;

Design outcomes

Primary

MeasureTime frame
The recurrence rate of keloids (defined as the appearance of skin elevation, congestion or obvious itching/pain beyond the original incision edge within the surgical incision range during the follow-up period, and it persists for more than one month without subsiding);

Secondary

MeasureTime frame
Vancouver Scar Scale (VSS) score (evaluating color, thickness, vascular distribution and softness);Patient-reported pain and pruritus score (VAS);RTOG skin injury classification (Evaluation of acute and late radiation-induced skin injury);

Countries

China

Contacts

Public ContactYu Daojiang

China National Nuclear Corporation 416 Hospital

ydj51087@163.com+86 28 84363381

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026