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Effect of two different dressings on palatal wound healing

Not Applicable
Completed
Conditions
Health Condition 1: null- Patients requiring free gingival graft for increasing width of attached gingiva or recession coverage
Registration Number
CTRI/2017/01/007719
Lead Sponsor
Institute of Dental Studies and Technologies
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

1)Systemically healthy patients aged 18 years or more,

2)Patient not under any medication for the past six months,

3)Patients requiring FGG either for reduced/ inadequate gingiva or gingival recession in the maxillary or mandibular anterior region,

4)Patients who have not undergone any palatal graft procedure in the past one year.

Exclusion Criteria

1)Smokers,

2)Pregnant or lactating mothers,

3)Patients not maintaining oral hygiene.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Immediate Bleeding <br/ ><br>Delayed Bleeding <br/ ><br>Pain Score <br/ ><br>Size of wound <br/ ><br>Depth of wound <br/ ><br>Toluidine blue test for epithelization <br/ ><br>Hydrogen peroxide test for epithelizationTimepoint: Immediate Bleeding:After suturing the donor area <br/ ><br>Delayed Bleeding: Between 1st â?? 7th Post operative days <br/ ><br>Pain Score, size, Toluidine blue test: 7th ,12th, 18th, 24th and 30th post-operative day. <br/ ><br>Depth of wound: Before surgery, immediately post surgery, post application of dressing and on 12th, 24th and 30th post-operative days. <br/ ><br>Hydrogen peroxide test for epithelialization: 7th & 8th, 12th &13th, 18th &19th, 24th &25th, 30th & 31st post-operative day. <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
oneTimepoint: None
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