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Most Preventable Surgical Option to Reduce Primary Spontaneous Pneumothorax Patients' Postoperative Recurrence: A Prospective Cohort Study

Most Preventable Surgical Option to Reduce Primary Spontaneous Pneumothorax Patients' Postoperative Recurrence: A Prospective Cohort Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04758143
Enrollment
450
Registered
2021-02-17
Start date
2020-08-11
Completion date
2025-03-31
Last updated
2021-02-18

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

Conditions

Recurrence, Spontaneous Pneumothorax, Surgery

Brief summary

To investigate the most preventable option to reduce primary spontaneous postoperative recurrence.

Detailed description

Pneumothorax is a disease in which air in the lungs leaks into the pleural cavity. It is a disease that occurs most often in young people with active social activities, and it occurs in about 100,000 people in 14 cases. The recurrence rate is as high as 17% to 54%, and the delay of the rehabilitation by the ambulatory with the treatment and prolongation of the hospitalization becomes a problem. It becomes a large failure for the youth who requires early rehabilitation. According to the latest report from the Japanese Society of Surgery, approximately 12,000 pneumothorax surgeries are performed annually in Japan. Many of them applied absorbent material to the surgical stump (coverage technique). However, there are no prospective studies, and efficacy does not appear adequately tested. It is necessary to accumulate prospective data from multiple centers to investigate the coverage technique's real effect.

Interventions

None listed

Sponsors

Yuka Kadomatsu
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

1. Patients who have spontaneous pneumothorax diagnosed by radiography and plan to underwent initial VATS bullectomy. 2. Patients who receive informed consent to attend this study, and the agreements are provided in a document. The consent of parents is also required, in case patients are under 20-years old.

Exclusion criteria

1. History of ipsilateral chest surgery. 2. Patients who only underwent exploratory surgery. 3. Patients who are judged ineligible by the investigator and the attending surgeon.

Design outcomes

Primary

MeasureTime frameDescription
Recurrence rate of pneumothoraxwithin 2 years after the surgeryRate of ipsilateral pneumothorax recurrence detected by radiography at two years after surgery

Countries

Japan

Contacts

Primary ContactYuka Kadomatsu, MD
ykadoamtsu@med.nagoya-u.ac.jp+81-52-744-2375
Backup ContactToyofumi Chen-Yoshikawa, PhD
tyoshikawa@med.nagoya-u.ac.jp+81-52-744-2375

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026