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Acute Phase Reaction clinical trials

View clinical trials related to Acute Phase Reaction.

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NCT ID: NCT05926089 Completed - Pneumonia Clinical Trials

Acute Phase Reactant in Non-COVID-19 Bacterial Pneumonia

Start date: October 1, 2020
Phase:
Study type: Observational

This study is a cross-sectional study, was conducted at Chest department of Kasr Al-ainy Hospital, Cairo university during the period between October 2020 and April 2021. The aim of the work was to evaluate levels of acute phase reactants(APR) in Non-COVID-19 bacterial pneumonia, and to correlate between levels of APR and the disease severity.

NCT ID: NCT05642117 Completed - Emergencies Clinical Trials

Pediatric Telephone Center Board 15

CTPC15
Start date: May 1, 2021
Phase:
Study type: Observational

This study evaluates the follow-up of advices given in a Urgent Medical Aid Service (SAMU 29) for every pediatric's emergency call under 15yo and try to evaluate the adhesion's factors.

NCT ID: NCT04838938 Completed - Treatment Clinical Trials

Personalized Medicine in Patients With Infective Endocarditis

Start date: March 1, 2021
Phase:
Study type: Observational [Patient Registry]

The hypothesis underlying this work is the identification of different sub phenotypes of patients with infective endocarditis through the study of the host's response to infection. Furthemore, metagenomic sequencing may be a helpful supplement to IE diagnostic, especially when conventional tests fail to yield a diagnosis.

NCT ID: NCT04383561 Completed - Inflammation Clinical Trials

Relationship Between LRG and Periodontal Disease

Start date: September 30, 2019
Phase: N/A
Study type: Interventional

This study aimed to investigate gingival crevicular fluid (GCF) and serum levels of LRG, interleukin (IL)-6 and tumor necrosis factor (TNF)-α in patients with periodontitis before and after non-surgical periodontal treatment.

NCT ID: NCT03375372 Completed - Periodontitis Clinical Trials

Effects of Periodontal Therapy on Markers of Acute Phase Response, Oxidative Stress

BCU2
Start date: April 11, 2003
Phase: N/A
Study type: Interventional

This study began enrollment in 2003 with final report completed in October of 2015. This submission is being provided to acquire an NCT number. This study was successfully executed according to protocol with full enrollment and completion of 89.7% of subjects. Subjects were enrolled into a two arm study 1) Combined therapy (scaling and root planing plus Crest products) vs. 2) delayed treatment. Subjects were followed for 6 months and a wide and extensive battery of biological samples were collected to determine the effects of treatment on the local and systemic inflammatory response.

NCT ID: NCT03122990 Completed - Hypertension Clinical Trials

Acute-phase Response & Periodontal Treatment in Patients With Hypertension

PERIO-HYPERTEN
Start date: June 1, 2016
Phase: N/A
Study type: Interventional

The aim of this study is to compare quadrant scaling and root planing (Q-SRP) versus full-mouth treatment (FM-SRP) in terms of acute-phase responses following non surgical periodontal treatment in patients affected by periodontitis and high blood pressure.

NCT ID: NCT03122977 Completed - Obesity Clinical Trials

Acute-phase Response & Periodontal Treatment in Obese Patients

PERIO-OBESE
Start date: June 1, 2016
Phase: N/A
Study type: Interventional

The aim of this study is to compare quadrant scaling and root planing (Q-SRP) versus full-mouth treatment (FM-SRP) in terms of acute-phase responses following no surgical periodontal treatment in obese patients affected by periodontitis.

NCT ID: NCT03087266 Completed - Diabetes Clinical Trials

Acute-phase Response & Periodontal Treatment in Diabetes Affected Patients

PERIO-DIA
Start date: June 1, 2016
Phase: N/A
Study type: Interventional

Thirty-eight periodontitis- and diabetes-affected subjects will be randomly allocated to non surgical periodontal treatment with either Full-Mouth Approach (FM-SRP) or Quadrant approach (Q-SRP). Patients will be seen one day and three months (study completion) after treatment. The 24 hours appointment will be occurring after the entire completion of the FM-SRP or the first quadrant of the Q-SRP. In the latter group other sessions of treatment will be performed within the following 3 weeks. At baseline, 24 hours and three months, anthropometric, inflammatory and endothelial parameters will be collected. Periodontal parameters will be checked at baseline and at three months. Main outcome of the study is the level of C-reactive protein 24 hours after treatment.

NCT ID: NCT02759965 Completed - Surgery Clinical Trials

Neuroinflammation and Cognitive Dysfunction After Orthopedic Surgery

Start date: September 1, 2014
Phase:
Study type: Observational

The primary hypothesis that orthopaedic surgery induces a neuroinflammatory response within 48 hours after elective hip or knee surgery and that there is an association between exaggerated CNS inflammatory response or impaired inflammatory resolution and postoperative cognitive dysfunction within one week and at three months postoperatively.

NCT ID: NCT02460926 Completed - Clinical trials for Periodontal Diseases

Acute Phase Response & Periodontal Treatment

PERIOSYST-1
Start date: May 2012
Phase: N/A
Study type: Interventional

This study has compared quadrant scaling and root planing (Q-SRP) versus intensive treatment performed within 24 hours (FM-SRP) in terms of acute phase responses following treatment of periodontal disease. The primary aim was to compare the differences in CRP acute increase following FM-SRP versus Q-SRP therapy (24 hours after therapy). Secondary outcomes included changes in a broad array of inflammatory and endothelial injury markers between groups. Patients were randomly assigned to either FM-SRP and Q-SRP. Data indicated that non-surgical periodontal therapy performed within 24 hours induced greater perturbations of systemic inflammation compared to conventional treatment.