Buccal fat pad versus palatal rotation scarf graft for soft tissue around zygomatic implants
Official title: Buccal Pad of Fat Graft vs. Palatal Rotation Scarf Graft for Soft Tissue Enhancement and Prevention of Dehiscence Around Zygomatic Implants Placed in Patients With Severely Atrophic Maxilla: A Randomized Clinical Trial
Run by Cairo University · NCT06968780 · Data updated 2026-11-12
We will test two grafting techniques—the buccal fat pad and the palatal rotation scarf—to see which better builds and stabilizes gum tissue around zygomatic implants in adults with severely atrophic upper jaws.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 8 (estimated) |
| Sponsor | Cairo University Academic / other |
| Drugs / interventions | radiation |
| Locations | 1 site (Cairo, Giza Governorate) |
| Status | Recruiting |
| Started | June 1, 2025 |
| Main results expected | July 1, 2026 |
| Study ends | December 1, 2026 |
| Registry record updated | December 12, 2025 |
| Trial ID | NCT06968780 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (≥18 years) with severely atrophic, edentulous upper jaws who are medically healthy (ASA I–II), motivated, and suitable candidates for zygomatic implant surgery are ideal.
✕Probably not a fit
Patients with contraindications to implant surgery (for example prior head/neck radiation, IV bisphosphonates, uncontrolled diabetes), heavy smokers, or those unable to undergo the required surgery are unlikely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study compares two soft-tissue grafting methods used during placement of zygomatic implants in patients with severely atrophic edentulous maxillae. Participants receive zygomatic implants and either a buccal fat pad graft or a palatal rotation scarf graft, and clinicians track soft tissue volume, tissue stability, and wound dehiscence over follow-up. Outcomes for tissue augmentation, complication rates, and clinical predictability will be compared between the two techniques. The aim is to identify the more reliable graft approach to support long-term success of upper-arch implant rehabilitation in challenging anatomy.
Why it matters
Potential benefit: If successful, the better-performing graft could reduce soft-tissue complications, improve tissue stability, and increase the long-term success of zygomatic implants.
How similar studies have gone: Both buccal fat pad and palatal rotation grafts have been used successfully in other oral surgeries, but direct head-to-head comparisons specifically around zygomatic implants are limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patient of age 18 years or more, who can understand and sign an informed consent. 2. Patients with severely atrophic edentulous upper arch (Cawood \& Howell class IV, V, VI) that could not be restored by standard axial implants without augmentation. 3. Patients with severely atrophic edentulous upper arch (Bedrossian classification inadequate bone in zones II or III or all three zones) that could not be restored by standard axial implants without augmentation. 4. Good systemic health (ASA score I-II) 5. Highly motivated patients with good compliance to oral hygiene habits. Exclusion Criteria: 1. Patients with cardiovascular disease or pulmonary disease or medical systemic condition that does not permit the surgical procedure under general anesthesia (ASA III, IV, V and VI). 2. Patients with conditions contraindicating implant placement (e.g.: radiation to the head and neck, intra-venous bisphosphonates, uncontrolled Diabetes mellitus). 3. Heavy smokers. (\> 20 cigarettes daily) 4. Patient with psychiatric problems, severe bruxism, or other parafunctional habits. 5. Acute maxillary sinus infection or untreated maxillary sinus cyst. 6. Malignancy or pathology in Maxilla or Zygoma.
Where it's running
-
Cairo University
Cairo, Giza Governorate, Egypt Recruiting
Study contacts
- Study coordinator: Khaled M Allam, DDS
- Email: khaled-allam@dentistry.cu.edu.eg
- Phone: +201122189816
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.