Skip to main content
Clinical Trials/CTRI/2024/03/064825
CTRI/2024/03/064825
Not yet recruiting
Phase 1

A randomised prospective clinical trial for evaluation of clinical effectiveness of autogenous tooth graft in socket preservation which is a clinical,radiological and histological study. - ATG

Tanya Singh0 sites0 target enrollmentTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Tanya Singh
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Tanya Singh

Eligibility Criteria

Inclusion Criteria

  • Age between 20 and 50 years.
  • Systemically healthy patients.ASA 1,ASA 2
  • Patients who require tooth extraction due to localized periodontitis,trauma and tooth fracture.
  • Patient having a tooth indicated for extraction which could be used for autograft.
  • Patient who received instruction on the purpose of the clinical study and gave his /her consent.

Exclusion Criteria

  • Systemic illness such as diabetes mellitus, cardiac diseases, immune\-compromised , patients taking medications such as corticosteroids, calcium channel blocker or bisphosphonates which are known to interfere with the outcome.
  • Pregnant and lactating patients.
  • Grossly decayed and RCT treated teeth
  • Alcoholics and Smokers.
  • Patients who demonstrate poor oral hygiene maintenance.
  • Patient who has received radiation therapy.
  • Patient who has acute infections.

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Phase 4
Prospective randomized clinical trial for evaluation of efficacy of Neurotropin in patients with lumbar spinal canal stenosis presenting with residual leg symptoms after decompression surgeryumbar spinal canal stenosis
JPRN-UMIN000001344Dept. of Orthopedic surgery, Keio University, School of Medicine60
Completed
Not Applicable
Prospective randomised trial to evaluate the effectiveness of hydrotherapy as opposed to dry land physiotherapySurgery: Disc surgerySurgeryDisc surgery
ISRCTN34262831Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)38
Completed
Not Applicable
aparoscopic-Assisted Psoas blockade: A novel post-operative analgesic technique in patients undergoing laparoscopic inguinal hernia repairPostoperative pain in patients undergoing inguinal hernia repairAnaesthesiology - AnaestheticsSurgery - Surgical techniquesOral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
ACTRN12615000632594Dr tarek Fouad Tammam46
Active, not recruiting
Not Applicable
Prospective randomised clinical trial to assess the efficacy of 70% v/v isopropyl alcohol and 2% w/v chlorhexidine in 70% v/v isopyl alcohol for the disinfection of skin prior to peripheral venous catheterisation. - Microbial contamination associated with ChloraPrep®
EUCTR2004-001086-17-GBMedi-Flex900
Completed
Not Applicable
A prospective randomised trial to examine the therapeutic effects of hydrotherapy in chronic rheumatoid arthritic patientsRheumatoid arthritis (RA)Musculoskeletal Diseases
ISRCTN58751336Arthritis Research Campaign (ARC) (UK)139