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NCT07381283
Immediate Versus Delayed Loading of Dental Implants in the Anterior Maxilla
NA trial testing Dental Implant in Partial Edentulism of the Maxilla in 16 participants. Completed in 12 October 2025.
21 May 2025
Quick facts
| Lead sponsor | Suez Canal University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 16 |
| Start date | 3 February 2024 |
| Primary completion | 21 May 2025 |
| Estimated completion | 12 October 2025 |
| Sites | 1 location across Egypt |
Drugs / interventions tested
- Dental Implant
Conditions studied
- Partial Edentulism of the Maxilla — all drugs for Partial Edentulism of the Maxilla →
- Dental Implant Loading — all drugs for Dental Implant Loading →
- Tooth Loss in the Anterior Maxilla — all drugs for Tooth Loss in the Anterior Maxilla →
Sponsor
Suez Canal University
Who can join
Adults 20 to 55, any sex, with Partial Edentulism of the Maxilla or Dental Implant Loading. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This interventional comparative clinical study was conducted to evaluate and compare the clinical stability and radiographic outcomes of immediate versus delayed loading of dental implants placed in the anterior region of the maxilla. Immediate loading protocols have been shown to improve oral health-related quality of life and patient satisfaction; however, their influence on implant stability and osseointegration remains an area of ongoing investigation. A total of sixteen dental implants were placed and the participants were randomly allocated into two equal groups using a computer-generated randomization method (www.Randomizer.org). In Group I (control group), eight implants were placed and restored following a delayed loading protocol, with prosthetic loading performed six months after implant placement. In Group II (study group), eight implants were placed and immediately loaded with provisional polymethyl methacrylate (PMMA) restorations. After six months, the provisional restorations were replaced with definitive fixed prostheses. Preoperative planning of implant placement was performed using cone beam computed tomography (CBCT). Clinical evaluation of implant stability was carried out using the Osstell device, while radiographic assessment of peri-implant bone density and marginal bone changes was performed using standardized indirect digital radiographs. Radiographic evaluations were obtained immediately after implant placement and at six months postoperatively. The clinical and radiographic outcomes of both loading protocols were compared to assess implant stability and osseointegration.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07381283
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Related trials
Other trials of Dental Implant
Trials testing the same drug.
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- NCT04695899 — Zirconia Implants for Replacement of a Single Tooth · active not recruiting
Other Suez Canal University trials
Trials by the same sponsor.
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- NCT07291791 — tDCS for Pain Modulation in Knee Osteoarthritis · NA · active not recruiting
- NCT07262086 — Clinical Evaluation of Wear Resistance and Bioactivity of Self Cured Bioactive Resin Composite · NA · enrolling by invitation
- NCT07125846 — Efficacy of Bioactive Glass vs. Xenograft in Maxillary Sinus Augmentation · NA · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07381283 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Suez Canal University
- Last refreshed: 2 February 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07381283.
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