NCT07022704

Brief Summary

Researchers aim to evaluate the impact of doxapram administration on diaphragmatic excursion in chronic obstructive pulmonary disease (COPD) patients undergoing spontaneous breathing trial

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
35

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 7, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 15, 2025

Completed
7 days until next milestone

Study Start

First participant enrolled

June 22, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2025

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2025

Completed
Last Updated

June 26, 2025

Status Verified

June 1, 2025

Enrollment Period

4 months

First QC Date

June 7, 2025

Last Update Submit

June 22, 2025

Conditions

Keywords

COPDDoxapramDiaphragmatic excursion

Outcome Measures

Primary Outcomes (1)

  • • Diaphragmatic excursion in mm

    before and 10 minutes after doxappram

Secondary Outcomes (2)

  • Arterial blood gases

    before and 10 minutes after doxapram

  • Respiratory rate

    before and 10 minutes after doxapram

Study Arms (1)

Doxapram

All patients will receive doxapram during spontaneous breathing trial

Drug: Doxapram

Interventions

Doxapram will be given as 1.5 mg/kg will be given 10 minutes after the initiation of SBT

Doxapram

Eligibility Criteria

Age20 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Chronic obstructive pulmonary diseases undergoing breathing trial

You may qualify if:

  • Patients with moderate to severe chronic obstructive pulmonary disease undergoing spontaneous breathing trial

You may not qualify if:

  • Refusal Allergy to doxapram neuromuscular disorders inability to evaluate the diaphragm

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cairo University

Cairo, Cairo Governorate, 6890, Egypt

RECRUITING

Related Publications (5)

  • Helmy MA, Magdy Milad L, Osman SH, Ali MA, Hasanin A. Diaphragmatic excursion: A possible key player for predicting successful weaning in patients with severe COVID-19. Anaesth Crit Care Pain Med. 2021 Jun;40(3):100875. doi: 10.1016/j.accpm.2021.100875. Epub 2021 Apr 30. No abstract available.

    PMID: 33940248BACKGROUND
  • Pourriat JL, Baud M, Lamberto C, Fosse JP, Cupa M. Effects of doxapram on hypercapnic response during weaning from mechanical ventilation in COPD patients. Chest. 1992 Jun;101(6):1639-43. doi: 10.1378/chest.101.6.1639.

    PMID: 1600786BACKGROUND
  • Oikawa S, Nomura H, Nishio M, Nagata R, Hata T. Doxapram hydrochloride aggravates adrenaline-induced arrhythmias accompanied by bidirectional ventricular tachycardia. ISRN Cardiol. 2014 Jan 9;2014:212045. doi: 10.1155/2014/212045. eCollection 2014.

    PMID: 24527224BACKGROUND
  • Rutka M, Palac M, Linek P. Diaphragmatic Mobility Loss in Subjects With Moderate to Very Severe COPD May Improve After In-Patient Pulmonary Rehabilitation. Respir Care. 2021 Feb;66(2):354. doi: 10.4187/respcare.08687. No abstract available.

    PMID: 33514664BACKGROUND
  • Scheibe N, Sosnowski N, Pinkhasik A, Vonderbank S, Bastian A. Sonographic evaluation of diaphragmatic dysfunction in COPD patients. Int J Chron Obstruct Pulmon Dis. 2015 Sep 11;10:1925-30. doi: 10.2147/COPD.S85659. eCollection 2015.

    PMID: 26392767BACKGROUND

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Interventions

Doxapram

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

PyrrolidinonesPyrrolidinesHeterocyclic Compounds, 1-RingHeterocyclic Compounds

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of anesthesia and critical care

Study Record Dates

First Submitted

June 7, 2025

First Posted

June 15, 2025

Study Start

June 22, 2025

Primary Completion

October 30, 2025

Study Completion

November 1, 2025

Last Updated

June 26, 2025

Record last verified: 2025-06

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