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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03078088
Other study ID # 201608805
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date June 15, 2017
Est. completion date February 27, 2019

Study information

Verified date March 2020
Source University of Iowa
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will be a randomized, cross-over study of THAM followed by saline or saline followed by THAM in human non-CF and CF subjects to assess nasal colonization


Description:

16 subjects per group will be randomized to receive study drug or saline followed by a wash out period and cross-over to the other treatment, three times daily for 4 days. Nasal swab will be done at baseline and after both study treatment and saline treatment for assessment of airway colonization.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date February 27, 2019
Est. primary completion date February 27, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 16 Years and older
Eligibility Healthy subjects:

Inclusion Criteria:

- 16 subjects, aged 16-80, clinically stable with no significant changes in health status for 14 days prior to Day 1, written informed consent obtained fom subject.

Exclusion Criteria:

- Pregnant or lactating

- Use of any investigational drug and/or participated in any interventional clinical trial within 28 days prior to screening, smoked in the last 6 months.

CF subjects:

Inclusion Criteria:

- FEV1% >35%, O2 saturation >90% on room air, clinically stable with no significant changes in health status for 14 days prior to Day 1, written informed consent obtained from subject.

Exclusion Criteria:

- Same as for healthy subjects.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Tham
alkalinizer
Saline
Placebo

Locations

Country Name City State
United States Univeristy of IOwa Iowa City Iowa

Sponsors (1)

Lead Sponsor Collaborator
Lakshmi Durairaj

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Nasal bacterial colonization Culture Day 5 of placebo or Tham intervention
Secondary Safety assessment questionnaire Questionnaire for local side effects Day 5 of placebo or Tham intervention
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