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临床试验/CTRI/2013/11/004155
CTRI/2013/11/004155已完成4 期

EFFICACY AND SAFETY OF INTRALESIONAL BLEOMYCIN IN COMPARISION TO COMBINATION OF INTRALESIONAL 5-FLUOROURACIL AND TRIAMCINOLONE ACETONIDE IN PATIENTS OF KELOID AND HYPERTROPHIC SCARS: A RANDOMISED, OPEN LABELLED, COMPARATIVE STUDY.

Government Medical College Bhavnagar1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2011年1月3日最近更新:

试验速览

阶段
4 期
状态
已完成
入组人数
60
试验地点
1
主要终点
change in pigmentation, vascularity, pliability and height of lesion using Vancouver’s scar scale.Score is based on the four parameters: pigmentation, vascularity, pliability and height of lesion. Total score is of 13. Pigmentation, vascularity and pliability will be assessed subjectively and the height is measured using vernier callipers.

研究概览

简要总结

This study is a randomized, open label, prospective, parallel group, single-centre  trail comparing the safety and efficacy of Sixteen intralesional injection of Inj.5-fluorouracil (50mg/ml) 0.9ml + inj. Triamcinolone acetonide(10mg/ml) 0.1ml will be given intralesionally weekly for 15 weeks in insulin syringe and upto 0.2ml of drug will be infiltrated till mild blanching occurs and Six intralesional injections, by tattooing method with insulin syringe 40 punctures/5 mm2 of Inj. Bleomycin (1.5mg/ml) given at 3 weekly for 15 weeks in 60 patients with keloids and hypertrophic scars ( 30 in each group) .study is being conducted at Sir. T. Hospital, Bhavnagar. The primary outcome measures is based on Vancouver scoring scale at every 3 weeks ( at 0, 3, 6, 9, 12 and 15 weeks). Score is based on the four parameters: pigmentation, vascularity, pliability and height of lesion. Total score is of 13. Pigmentation, vascularity and pliability will be assessed subjectively and the height is measured using vernier callipers.  The secondary outcomes is based on the scale for the patient self assessment scar scale, photograph evaluation and global evaluation. Patient self assessment scar Scale is consisted of six parameters: pain, itching, colour, stiffness, thickness, and psychological discomfort. Total score is of 18. This scale will be taken at every 3 weeks (at 0, 3, 6, 9, 12 and 15 weeks).

Adverse events will be monitored throughout the study period during each visit by Clinical evaluation for the development of dermal atrophy, skin pigment changes, minor ulcerations, swelling, pain, erythema, telengiectasias, molting, anemia, leucopenia, thrombocytopenia, and pulmonary fibrosis; and Laboratory evaluation using Hematological parameters: Hb, TC, DC, RBC count, Platelet count, ESR; RBS; Renal function test: S.creatinine, B.urea; Liver function test: S.bilirubin SGPT, SGOT, ALP ) will be performed at the baseline and thereafter every 3 weeks up to 15 weeks. The chest X-ray will be taken at baseline and after 15 weeks.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Open Label

入排标准

年龄范围
15.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • patients with keloid or hypertrophic scar with •No history of treatment taken for keloids or hypertrophic scar for at least 3 months.
  • •Scar size less than or equal to 15 cm in all dimensions.
  • •Scar duration more than or equal to 6 weeks.

排除标准

  • •pregnant women •nursing mothers •pre-existing cardiac disease •uncontrolled hypertension •uncontrolled diabetes mellitus •Autoimmune diseases •Bleeding disorders •Pulmonary fibrosis.

结局指标

主要结局

change in pigmentation, vascularity, pliability and height of lesion using Vancouver’s scar scale.Score is based on the four parameters: pigmentation, vascularity, pliability and height of lesion. Total score is of 13. Pigmentation, vascularity and pliability will be assessed subjectively and the height is measured using vernier callipers.

时间窗: every 3 weeks (at 0, 3, 6, 9, 12 and 15 weeks).

次要结局

  • Scale for patient self assessment of scar,, photograph evaluation and global evaluation. Patient self assessment scar Scale is consisted of six parameters: pain, itching, colour, stiffness, thickness, and psychological discomfort. Total score is of 18.(every 3 weeks (at 0, 3, 6, 9, 12 and 15 weeks).)

研究者

申办方类型
Government medical college

研究点 (1)

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