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Data collection study on pharyngeal findings in streptococcal infections

Data collection study on pharyngeal findings in streptococcal infections

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs032190124
Enrollment
200
Registered
2019-10-28
Start date
2019-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Streptococcal infection

Interventions

Sponsors

kato Yuji
Lead Sponsor
Aillis Inc
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) A person who has obtained the written consent of the individual or his (her) proxy (parent) freely in clinical research participation (2) A person who is 6 years old or older at the enrollment (age that can use the tongue depressor that is a component of the medical device under development) For pediatric patients, carefully consider your understanding of the research content in consideration of the physique. (3) Persons who fall into one or more of the following 1) to 5) [excluding those who have chronic symptoms (those that have persisted for more than one week) for 1) to 4)] 1) With a fever of 37.0 degrees or higher (including cases that exceeded 37 degrees in home measurements) 2) Redness, white moss or swelling of tonsils 3) Cervical lymph node enlargement or tenderness 4) Sore throat 5) Patients whose doctor considers the possibility of streptococcal infection such as exposure to streptococcal patients

Exclusion criteria

Exclusion criteria: (1) Person who has swing tooth (2) Persons with severe lesions in the oral cavity where clinical research equipment comes into contact (3) Those who have severe nausea and have been judged by a physician as inappropriate to use clinical research equipment (4) Persons who have difficulty in taking the open position with clinical research equipment (eg, small body size, clinical research equipment cannot be inserted into the mouth, pain such as temporomandibular disorders, or difficulty in maintaining the open position due to poor compatibility of dentures, etc. ) (5) Persons who are scheduled to participate in other clinical trials (except post-marketing surveillance) between the date of consent acquisition and the end of the trial period, and those who are unable to comply with the clinical study implementation plan and follow-up For social, family, social, geographical reasons) (6) Those who have a clear understanding of this study among pediatric patients. Also, those who are small in size and cannot insert clinical research equipment into the oral cavity. (7) Other persons who are judged inappropriate by the doctor responsible for clinical research

Contacts

Public ContactYuji Kato

TSUKISHIMA E.N.T clinic

yujik.ent@gmail.com+81-3-3533-1333

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026