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NCT05709236
Digital Versus Conventional Full-arch Implant Impression in Maxillary Screw- Retained Implant Prosthesis
NA trial testing Maxillary screw-retained prosthesis in Jaw, Edentulous in 28 participants. Completed in 10 August 2022.
10 May 2022
Quick facts
| Lead sponsor | Delta University for Science and Technology |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 28 |
| Start date | 5 January 2020 |
| Primary completion | 10 May 2022 |
| Estimated completion | 10 August 2022 |
| Sites | 1 location across Egypt |
Drugs / interventions tested
- Maxillary screw-retained prosthesis
Conditions studied
- Jaw, Edentulous — all drugs for Jaw, Edentulous →
Sponsor
Delta University for Science and Technology
Who can join
Adults 56 to 70, any sex, with Jaw, Edentulous. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
28 participants with edentulous maxillary arches were randomly selected and enrolled in two equal groups; Group I conventional impression group (CIG) and Group II Digital impression group (DIG). All patients were rehabilitated with maxillary screw-retained implant prosthesis retained by 6 implants. Prosthodontic complications and peri-implant MBL were registered at 6,12, and 24 months (m). Data was collected and statistically analyzed.
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 NCT05709236
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Jaw, Edentulous
Currently open trials in the same condition.
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Other Delta University for Science and Technology trials
Trials by the same sponsor.
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- NCT07292675 — The Effect of Low Intensity With BFR on Stroke Patients · NA · not yet recruiting
- NCT07230938 — Effects of Neck Proprioception Impairment on Balance in Cervical Spondylosis Patients · not yet recruiting
- NCT07333872 — Evaluation of Pulpotomy, Partial Pulpotomy, and Direct Pulp Capping Using Mineral Trioxide Aggregate. · NA · active not 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 NCT05709236 (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 Delta University for Science and Technology
- Last refreshed: 2 February 2023
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/NCT05709236.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing