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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02091258
Other study ID # UCL 14/0110
Secondary ID
Status Active, not recruiting
Phase N/A
First received March 17, 2014
Last updated September 26, 2017
Start date June 2014
Est. completion date December 2020

Study information

Verified date September 2015
Source University College, London
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Tooth loss in periodontitis patients is associated with patient and site factors as well as with treatment provided. Not much is known about long-term tooth loss in periodontitis patients in private practice in the UK. The study plans to follow-up 200 subjects with periodontitis (and currently on maintenance therapy) for 5 years. The effect of treatment provided, site and patient risk factors on tooth loss will be studied.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 200
Est. completion date December 2020
Est. primary completion date May 2020
Accepts healthy volunteers No
Gender All
Age group 16 Years to 75 Years
Eligibility INCLUSION CRITERIA:

1. Initial diagnosis of chronic or aggressive periodontitis (Lindhe et al. 1999, Lang et al. 1999), with at least two sites with PPD and CAL =5mm

2. Diagnosed and treated by the same periodontist (LN)

3. Willing to give written informed consent for study participation

4. Willing to undergo SPT as per standard of care for at least 5 years

EXCLUSION CRITERIA:

1. Serious medical history that prevents patients from undergoing dental treatment

2. History of rheumatic fever, heart murmur, mitral valve prolapse, artificial heart valve or other conditions requiring prophylactic antibiotic coverage prior to invasive dental procedures

3. Current alcohol or drug abuse

4. Self-reported pregnancy or lactation

5. Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may compromise trial participation and/or interpretation of trial results and, in the judgement of the investigator, would make the subject inappropriate for entry into this trial

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom The Dentist Bishop's Stortford Herts
United Kingdom Ravenscourt Dental Practice London

Sponsors (1)

Lead Sponsor Collaborator
University College, London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tooth loss 5 years
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