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Effect of Vitamin D Application on Bone Loss Around Dental Implants A Clinical Study

Comparative Evaluation of Crestal Bone Loss in Delayed Implant Placement With or Without Topical Vitamin D Application in Osteotomy Site A Randomized Controlled Clinico-CBCT Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112269
Enrollment
20
Registered
2026-06-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K068- Other specified disorders of gingiva and edentulous alveolar ridge

Interventions

Intervention1: Topical Vitamin D application in delayed implant placement: Patients undergoing delayed implant placement are allocated into two groups In the test group Vitamin D is applied topically

Sponsors

Subharti Dental College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having a single missing tooth with an adequate mesiodistal width and vertical bone height of the edentulous site available for placement of an implant Edentulous sites in mandibular or maxillary arches Adjacent teeth intact restored with functionally and esthetically good restorations restored with a prosthesis precluding the addition of the missing tooth Patients with good periodontal status and general systemic health

Exclusion criteria

Exclusion criteria: Patients who are unable to perform routine oral hygiene procedures Patients with a history of smoking Patients with TMJ disorders Patients with a dental history of bruxism and parafunctional habits or deep bite cases History of substance abuse Insufficient vertical inter arch spaces to accommodate the prosthodontic components available together with a proposed pontic and occasional gingival analogue designs Patients with uncontrolled diabetes Absence of opposing occlusion

Design outcomes

Primary

MeasureTime frame
Crestal bone loss in mm around delayed implant sites assessesd using CBCT imagingTimepoint: Baseline 3 months postoperatively and 6 months postoperatively

Secondary

MeasureTime frame
Implant stability peri implant soft tissue parameters postoperative healing pain assessment and complications Timepoint: Baseline 1 week 1 month 3 months and 6 months

Countries

India

Contacts

Public ContactDr Ritika Singh

Subharti Dental College Swami Vivekanand Subharti University

drmayurkaushik@gmail.com9759444434

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026