Clinical Study of Kangfuxin and Basic Fibroblast Growth Factor in Promoting the Healing of Donor Site

NCT04234321 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2020-05-12

No results posted yet for this study

Summary

The main objective of this study is to observe whether basic fibroblast growth factor and Kangfuxin Liquid can promote the wound healing in the donor area and further evaluate the healing quality.

Conditions

  • Fibroblast Growth Factors
  • Wound Healing

Interventions

DRUG

basic fibroblast growth factor

Basic fibroblast growth factor,100ml/ bottle, (35000IU / 8ml) / 100cm2 / time,three times a day.

DRUG

Kangfuxin Liquid

Kangfuxin Liquid,20ml / 100cm2 / time,three times a day.

DRUG

0.9% Normal saline

0.9% Normal saline,20ml / 100cm2 / time,three times a day.

Sponsors & Collaborators

  • The Second Affiliated Hospital of Kunming Medical University

    collaborator OTHER
  • Jiangyin Hospital Affiliated to Southeast University School of Medicine

    collaborator UNKNOWN
  • Nantong University

    collaborator OTHER
  • The 59th Central Hospital of the Chinese people's Liberation Army

    collaborator UNKNOWN
  • Taizhou Hospital

    collaborator OTHER
  • Zhejiang Quhua Hospital

    collaborator OTHER
  • Lishui Country People's Hospital

    collaborator OTHER
  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    lead OTHER

Principal Investigators

  • huawei shao, MD · 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-08-01
Primary Completion
2022-06-30
Completion
2022-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04234321 on ClinicalTrials.gov