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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05334745
Other study ID # 01005007001
Secondary ID
Status Recruiting
Phase Phase 1
First received
Last updated
Start date December 1, 2021
Est. completion date January 1, 2023

Study information

Verified date April 2022
Source Cairo University
Contact mohy eldin aboelazayem, TA
Phone +201005007001
Email mohy.aboelazayem@dentistry.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to evaluate the effect of application of Alvogyl versus hyaluronic acid in decreasing postoperative pain and promoting healing in the palatal wound following the free gingival graft procedure


Description:

Postoperative pain and bleeding are the most common complications after palatal graft harvesting, also postsurgical swelling have been reported. Although hemostatic agents, mechanical barriers, bioactive materials, antibacterial and antiseptic agents and herbal products have been found effective in preventing such complications, an ideal support could not be specified for this purpose. Further, undesired side effects such as delayed wound healing/foreign body reaction have been reported . No gold standard has been identified, thus there is a need for further investigations aiming to reach the best possible treatment modality for pain relief and prevention of reported complications following harvesting of palatal graft .


Recruitment information / eligibility

Status Recruiting
Enrollment 16
Est. completion date January 1, 2023
Est. primary completion date December 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Patients with mucogingival defects scheduled for free gingival graft - Age from 18 years up to 60 - Medically healthy patient Exclusion Criteria: - Systemic diseases that may be a contraindication for any surgeries. - Loss of maxillary premolars and molars. - Pregnancy or lactation - Smoking

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Alvogyl
application of Alvogyl in the palatal wound with stent versus hyaluronic acid application

Locations

Country Name City State
Egypt Egypt Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain Pain through one week using the visual analogue scale (VAS) 7th days
Secondary Wound healing Wound healing index through one month .
The healing index has 5 grades which are 5(excellent healing), 4(very good healing), 3 (good healing), 2(poor healing) and 1(very poor healing)
7th, 14th, 21st and 30th days.
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