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NCT01628367
The Effectiveness of the Cytoplast Technique in Preventing Bone Loss Around Immediate Implant Placement in the Esthetic Zone. A Randomized Clinical Trial.
Phase 4 trial testing Minimally Traumatic Tooth Extraction in Missing Tooth in 32 participants. Completed in 1 May 2014.
1 May 2014
Quick facts
| Lead sponsor | University of Michigan |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 32 |
| Start date | 1 July 2012 |
| Primary completion | 1 May 2014 |
| Estimated completion | 1 May 2014 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Minimally Traumatic Tooth Extraction
- Immediate Implant Placement
- Bone Graft Placement — full drug profile →
- Membrane placement — full drug profile →
- Collagen plug placement — full drug profile →
- Medications — full drug profile →
Conditions studied
- Missing Tooth — all drugs for Missing Tooth →
Sponsor
University of Michigan
Who can join
Adults 18 to 100, any sex, with Missing Tooth. Healthy volunteers can join.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Change in Thickness of Buccal Bone
Time frame: One year
Change of buccal bone volume over study duration
Sponsor's own description
An important result of healing after tooth extraction is a reduction in dimensions of the remaining bone at that site. This reduction of bone volume precludes successful restoration of the space using a dental implant. Bone augmentation has shown promise in clinical reports to reduce this loss of bone volume, thus allowing implant placement and restoration. The purpose of this study is to evaluate the clinical and radiographic outcomes of guided bone regeneration around dental implants placed in fresh extraction sockets.
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 NCT01628367
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT01628367 (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 University of Michigan
- Last refreshed: 10 February 2017
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/NCT01628367.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing