- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07683741
Hydrolyzed Collagen As A Host Modulation Agent in Non-Surgical Periodontal Treatment
Investigation of the Host Modulator Efficacy of Food Supplement Containing Hydrolyzed Collagen in Non-Surgical Periodontal Treatment of Patients With Periodontitis
This study was planned on the basis of the hypothesis that 'food supplements containing collagen will support the clinical effectiveness of non-surgical periodontal therapy'. In this context, the aim of the study is to investigate the therapeutic efficacy of collagen-containing food supplement as a host modulation agent in the non-surgical periodontal treatment of individuals with stage 3-4 periodontitis in a clinical and biochemical manner in a comprehensive manner.
Initial day: Anamnesis, diagnosis and index measurements 2 days later, collection of serum samples from the patient, oral hygiene training and straightening of the whole mouth root surface and cleaning of the whole mouth tooth surface The next day, full mouth scalling and root planing are closed with the second session and tablets are started.
End of 2nd month:
Periodontal index measurement and oral hygiene training Collecting serum and tissue samples 2 days later
End of 6th month Periodontal index measurement and oral hygiene training Collecting serum and tissue samples 2 days later
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
Rize Province
-
Rize, Rize Province, Tyrkia (Türkiye), 53000
- Recep Tayyip Erdogan University
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- 18 - 60 age
- stage 3-4 periodontitis
Exclusion Criteria:
- Patients who smoke more than 10 cigarettes a day
- Patients using immunosuppressive, oral contraceptive, bisphosphonate drugs
- Patients who are during pregnancy or lactation
- Having undergone periodontal treatment in the last 6 months, having used antibiotic anti-inflammatory medication in the last 4 weeks
- The presence of any autoimmune disease, osteoporotic disease or cancer disease
- Patients with renal and hepatic insufficiency
- Patients with thyroid dysfunction
- The presence of active infectious diseases(acute hepatitis, tuberculosis, AIDS)
- Chronic drug use affecting periodontal tissues(cyclosporine A, Phenytoin)
- Intake of antioxidant supplements
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Støttende omsorg
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Placebo komparator: placebo gruppe
|
placebo will be given.
|
|
Aktiv komparator: Patients using collagen peptides
|
Collagen supplements will not be given in the placebo group.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
probing pocket depth
Tidsramme: baseline, 1st month and 3rd month
|
The distance between the gingival margin and the pocket base was measured in millimeters.
|
baseline, 1st month and 3rd month
|
|
clinical attachment loss
Tidsramme: baseline, 1st month and 3th month
|
The distance from the enamel-cementum junction to the pocket base was measured in millimeters.
|
baseline, 1st month and 3th month
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
assessment of interleukin-1 beta levels
Tidsramme: baseline, 1st month and 3th month
|
Serum interleukin-1 beta levels were measured biochemically.
|
baseline, 1st month and 3th month
|
|
assessment of matrix metalloproteinase-8 (MMP-8) levels
Tidsramme: baseline, 1st month and 3 th month
|
Matrix metalloproteinase-8 (MMP-8) levels in gingival crevicular fluid were measured biochemically.
|
baseline, 1st month and 3 th month
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- RTEU Collagen Preparate
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
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