NCT07484685 Reduced Time Interval for Implant Placement After Extraction Socket Preservation Using the Vega Plus Implants
| NCT ID | NCT07484685 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Universidad Catolica Santiago de Guayaquil |
| Condition | Alveolar Bone Loss |
| Study Type | INTERVENTIONAL |
| Enrollment | 40 participants |
| Start Date | 2026-02-28 |
| Primary Completion | 2026-12-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 40 participants in total. It began in 2026-02-28 with a primary completion date of 2026-12-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This randomized controlled clinical trial aims to evaluate whether reducing the healing interval for implant placement after extraction socket preservation improves clinical and radiographic outcomes compared with the conventional waiting period. Participants requiring single-tooth extraction and implant therapy will be randomly assigned to implant placement either 4 months or 6 months after ridge preservation using the Vega Plus implant system (Klockner). Clinical and radiographic assessments will be performed at baseline and during follow-up visits. The primary outcome will be the mean change in horizontal alveolar ridge width measured using cone-beam computed tomography (CBCT). Secondary outcomes will include vertical bone height changes measured on CBCT, implant stability measured using resonance frequency analysis (ISQ values), marginal bone level changes assessed on standardized periapical radiographs, and postoperative pain assessed using the Visual Analog Scale (VAS). The results of this study may contribute to optimizing treatment timing and improving efficiency in implant dentistry while maintaining favorable clinical outcomes.
Eligibility Criteria
Inclusion Criteria: * Age: ≥ 18 years. * Good general health. * Need of extraction of incisors, canines or premolars due to carious lesion, endodontic complication, root fracture or prosthetic reason. * Presence of three intact socket walls after tooth extraction with a defect of 50% or more of the buccal wall. * Need of single-tooth implant treatment, with presence of adjacent teeth and opposing occluding teeth (for measurement stent indexing). * Enough available bone assessed on CBCT to place implants with 3.6 mm diameter and 10 mm in length. * Periodontal health in intact or reduced periodontium. * Full-mouth plaque and bleeding scores \< 20%. * Able and willing to follow study procedures and instructions. Exclusion Criteria: * \< 18 years. * Compromised health. Existence of any systemic condition such as uncontrolled diabetes mellitus, cancer, HIV, disorders that compromise wound healing, chronic high dose steroid therapy, intravenous and oral bisphosphonate therapy, bone metabolic diseases, history of irradiation of the head and neck area, or any other immunosuppressive therapy that would contraindicate oral surgical treatment. * Absence of any adjacent teeth or the opposing occluding teeth. * The hopeless tooth is a molar.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07484685 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Alveolar Bone Loss. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07484685 currently recruiting?
Yes, NCT07484685 is actively recruiting participants. Contact the research team at gabriela.manzaba30@gmail.com for enrollment information.
Where is the NCT07484685 trial being conducted?
This trial is being conducted at Guayaquil, Ecuador.
Who is sponsoring the NCT07484685 clinical trial?
NCT07484685 is sponsored by Universidad Catolica Santiago de Guayaquil. The trial plans to enroll 40 participants.