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Evaluating the impact of Halotherapy on improving pulmonary tests results and status of patients with Chronic Obstructive Pulmonary Disease referred to Dr. Masih Daneshvary hospital of Tehran in 2016 to 2017

Evaluating the impact of saturated steam with salt in improving pulmonary tests results and status of patients with Chronic Obstructive Pulmonary Disease attend in Dr. Masih Daneshvary hospital of Tehran in 1395 to 1396

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016080927995N2
Enrollment
84
Registered
2016-11-26
Start date
2016-09-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic obstructive pulmonary disease. Chronic obstructive: airway disease NOS lung disease NOS

Interventions

Intervention 1: A kind of inhalation therapy with a mineral salt as an alternative treatment named halotherapy twice a day each for 30 minutes for 2-months. Intervention 2: Patients in control group
Treatment - Drugs
Placebo
A kind of inhalation therapy with a mineral salt as an alternative treatment named halotherapy twice a day each for 30 minutes for 2-months
Patients in control group use plastic contained Saltairs which have no inhaler in it actually as placebo drug.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: COPD patients regarding GOLD criteria; Stable patients older 18 years . Exclusion criteria: History of surgery in thorax; COPD exacerbation; Unbearable complications of COPD; Huge changes in treatment regimen; Missing patients through out the study; Irregular treatment; Smoking; Exacerbation in comorbidities like CHF, CRF, etc.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The walked distance. Timepoint: two month after first visit. Method of measurement: 6MWT.;Forced vital capacity. Timepoint: two month after study beginning. Method of measurement: spirometry.;Forced expiratory volume. Timepoint: two month after study beginning. Method of measurement: spirometry.;Minute. Timepoint: 2 month after first visit. Method of measurement: 6MWD.

Secondary

MeasureTime frame
Disease manifestation. Timepoint: 2 month after first visit. Method of measurement: Asking patients.;Exacerbation rate. Timepoint: Every other month. Method of measurement: Asking patients.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Eslaminejad

Shahid Beheshti University of Medical Sciences

eslaminejadalireza@yahoo.com+98 21 2610 9647

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026