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NCT05808062
The Effect of Canal Dryness on the Quality of Obturation
NA trial testing Root canal obturation in Obturation in 24 participants. Completed in 31 December 2022.
1 December 2022
Quick facts
| Lead sponsor | British University In Egypt |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 24 |
| Start date | 1 January 2022 |
| Primary completion | 1 December 2022 |
| Estimated completion | 31 December 2022 |
| Sites | 1 location across Egypt |
Drugs / interventions tested
- Root canal obturation
Conditions studied
- Obturation — all drugs for Obturation →
Sponsor
British University In Egypt
Who can join
Adults 23 to 25, any sex, with Obturation. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this clinical trial is to evaluate root canal obturation quality. The questions to answer are * what is the best protocol for canal dryness before obturation ? * Is compaction necessary ? Volunteer participants will perform root canal treatment in teeth planned for extraction due to orthodontic reasons
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Ex-vivo evaluation of clinically-set hydraulic sealers used with different canal dryness protocols and obturation techniques: a randomized clinical trial.
Nawar NN, Elashiry MM, El Banna A, Saber SM, et al · · 2024 · cited 2× · PMID 39463194 · DOI 10.1007/s00784-024-06006-5
Verify or expand the search:
- PubMed search for NCT05808062
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Root canal obturation
Trials testing the same drug.
- NCT05739682 — Pain and Microbial Reduction of Antimicrobial Corticosteroid Mixture Versus Cryotherapy in Necrotic Teeth · NA · completed
- NCT04482101 — Single Visit Root Canal Treatment :Incidence of Postoperative Pain Using Two Different Sealers · NA · unknown
- NCT03636087 — Impact of an Enhanced Sterile Protocol on Root Canal Treatment Outcome · NA · unknown
Other British University In Egypt trials
Trials by the same sponsor.
- NCT07492576 — Evaluation of the Magnesium Shield Compared to Dual Zone Grafting Approach in Immediate Implant Site Management · NA · recruiting
- NCT07457749 — Clinical Performance of a Novel Self-cured Resin Composite Compared to a Light-cured Bioactive Resin Composite Restorati · EARLY_PHASE1 · recruiting
- NCT07368621 — Effectiveness of Connective Tissue Graft With and Without Leukocyte Platelet Rich Fibrin on Peri-implant Soft Tissue Thi · NA · recruiting
- NCT07480070 — Two-Year Clinical Performance of Self-Cured Resin Composite in Comparison to Light-Cured Bioactive Resin Composite in Re · NA · completed
- NCT07115758 — Vestibular Versus Trapezoid Flap in Immediate Implants · 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 NCT05808062 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by British University In Egypt
- Last refreshed: 3 August 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/NCT05808062.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing