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Completed

NCT Number: NCT05513222

Flipped Autograft for Treating Surgical Wound Dehiscence

This case report describes a novel technique for management of peri-implant wound dehiscence that involves using auto graft from the same surgical site to seal the dehiscence defect.

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Key information

Conditions

Wound Dehiscence

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ahmed Hamdy

Cairo, 11837, Egypt

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients in a healthy systemic condition.
  • Both genders
  • Patients should have single missing tooth.
  • Seibert Class I ridge defect.
  • Patients should approve to deliver a signature to a written consent after study nature explanation.

Exclusion criteria

  • 1- Patients with any smoking habits. 2- Pregnant females, decisional impaired individuals, Prisoners and handicapped patients.

3- Patients having poor oral hygiene or not wanting to carry out oral hygiene measures.

4- Patients with infections either periodontally or periapically.

Treatment and study plan

flipped autograft

Procedure

Thick lingual flap was de-epithelized and partially dissected to increase its length then flipped and sutured to the buccal flap to obtain primary closure

Primary outcomes

  1. complete primary intention healing of the wound dehiscence

    Time frame: 3 months

    complete uneventful healing will be assessed clinically by measuring soft tissue width and thickness using periodontal probe under local anesthesia

Secondary outcomes

  1. esthetic outcome and patient satisfaction.

    Time frame: 3 months

    esthetic outcome will be measured using pink esthetic score. Pink esthetic score (PES) will be recorded for five variables: "mesial papilla, distal papilla, curvature of the facial mucosa, level of the facial mucosa, and root convexity/soft tissue color and texture at the facial aspect of the implant site". A score of 2, 1, or 0 will be assigned to all five parameters.

    also patient satisfaction will be recorded using:

    • (VAS) Visual analogue scale to measure postoperative pain. Pain score reported by the patient. directly through Visual Analogue Scale score (from 0 to 10. 0: no pain, 1: minimal pain, 5: moderate pain, 10: severe pain) which will be recorded after 2 weeks (Yildirim et al., 2017)

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Collaborators

  • British University In Egypt

Registry information

Official study title

Flipped Autograft: a Novel Approach for Management of Wound Dehiscence in Implant Dentistry

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Aug 24, 2022
Registry last updated
Apr 2, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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