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NCT04353362
Alternative Antibiotic Regimen in Periodontitis Treatment
Phase 4 trial testing Ofloxacin in Amoxicillin in 74 participants. Completed in 10 March 2020.
2 January 2020
Quick facts
| Lead sponsor | Istanbul Medipol University Hospital |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | supportive care |
| Enrollment | 74 |
| Start date | 1 April 2017 |
| Primary completion | 2 January 2020 |
| Estimated completion | 10 March 2020 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Ofloxacin (OFLOXACIN) — full drug profile →
- Amoxicillin (amoxicillin) — full drug profile →
- Metronidazole (METRONIDAZOLE) — full drug profile →
Conditions studied
- Amoxicillin — all drugs for Amoxicillin →
- Metronidazole — all drugs for Metronidazole →
- Ofloxacin — all drugs for Ofloxacin →
- Periodontitis — all drugs for Periodontitis →
Sponsor
Istanbul Medipol University Hospital
Who can join
Adults 20 to 40, any sex, with Amoxicillin or Metronidazole. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Context and Aims: Several studies have demonstrated an association between obesity, periodontitis, and exercise. This study aimed to investigate the effects of regular exercise on obese women with periodontal disease, using serum, saliva, and gingival crevicular fluid (GCF) samples. Settings and Design: A before-after study design was adopted to evaluate the effects of 12 weeks of regular exercise on obese women grouped according to periodontal status, without a control group (no exercise). Methods and Material: The study sample comprised fifteen patients without periodontitis (NP group) and 10 patients with chronic periodontitis (CP group), from whom periodontal parameters were measured and serum, saliva, and GCF samples were collected. Body mass index (BMI), anthropometric measurements, somatotype-motoric tests, and maximal oxygen consumption (VO2max) were recorded at baseline and after exercise. Statistical analysis used: MedCalc was used for statistical analysis.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04353362
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Related trials
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Other Istanbul Medipol University Hospital trials
Trials by the same sponsor.
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- NCT07468864 — Validity of the Turkish Situational Vertigo Questionnaire · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04353362 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Istanbul Medipol University Hospital
- Last refreshed: 20 April 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04353362.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing