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To compare the effect on surrounding structures by two different joints between artificial root and artificial tooth

Evaluation of peri implant soft and hard tissues between internal hexagonal and internal conical type of implant abutment connection- A randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/01/030194
Enrollment
44
Registered
2021-01-01
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: K084- Partial loss of teeth

Interventions

Intervention1: Delayed occlusal loading of implants placed in properly healed single teeth edentulous site: After delayed occlusal loading, the peri-implant tissue is evaluated for next 12 months Cont

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient in the age group of 18years or above who will be able to understand the procedure and be able to provide informed consent to participate in it. 2. Partially edentulous in posterior region(molar and premolar). 3. Patients with simplified oral hygiene index score less than 3 4. Patients having sufficient bone to allow optimal implant placement without the need of bone augmentation or recontouring and having sufficient distaance from vital tissues(2mm). 5. Presence of keratinized tissue more than 2mm 6. Stable posterior occlusion 7. Presence of adjacent teeth (1.5mm)

Exclusion criteria

Exclusion criteria: 1. Patient with a history of systemic disease that precludes standard implant therapy. 2. Patients having parafunctional habits 3. Patient with a current daily smoking habit or chewing tobacco and with a history of drug abuse or alcoholism within past years 4. Pregnant or lactating mother

Design outcomes

Primary

MeasureTime frame
Levels of Crestal bone loss Levels of IL-1beta Change in probing depth Change in bleeding on probing indexTimepoint: parameters will be recorded during the time of delivery of prosthesis 3 months after occlusal loading 6 months after occlusal loading 12 months after occlusal loading

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactRamashanker Siddarth

King Georges Medical College, U.P.

aditiara33@gmail.com7599114676

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026