Pelvic FracturePELVICOELIONCT05836727
Use of Laparoscopy in the Treatment of Pelvic Ring Ruptures
An observational study of Pelvic Fracture, run by University Hospital, Brest at 1 site in France.
Trial summary
Case series to describe the use of laparoscopy for the treatment of pelvic ring disruption. Read more about this study
- Who is it for?
- Ages 18 to 100 years
- Conditions the study is for
- Pelvic Fracture
- How many people
- 14 participants
- Where
- 1 siteFrance
- Study dates
- 1 Mar 2023to 1 Jun 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 100 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: patients who underwent laparoscopy for the treatment of pelvic ring disruption
Who may be able to join
- patients who underwent laparoscopy for the treatment of pelvic ring disruption
Who cannot join
- patient < 18 years old
Trial locations and contacts
1 site in 1 country.
About this study
Case series to describe the use of laparoscopy for the treatment of pelvic ring disruption.
- Conditions
- Pelvic Fracture
- Keywords
- Pelvic ring surgery, Trauma Surgery, Plate Fixation, Laparoscopy, Case series
- Medical subject headings
- Hip Fractures
What is being measured
The primary outcome is the main question the study is designed to answer.
conversion rate to open surgery
conversion rate to open surgery
Measured: intraoperative
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 May 2023
- Study start1 Mar 2023
- Primary completion1 Apr 2023
- Study completion1 Jun 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pelvic FractureStudies of the same condition, open and under way.
- More trials run by University Hospital, BrestThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 14 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Brest
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05836727
- Sponsor's protocol ID
- 29BRC23.0010 - PELVICOELIO
- Acronym
- PELVICOELIO
- Status last verified
- Feb 2023
- First submitted
- 19 Apr 2023
- Last updated
- 1 May 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: All collected data that underlie results in a publication
Study at a glance
From the registry record, last updated by the sponsor on 1 May 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Use of Laparoscopy in the Treatment of Pelvic Ring Ruptures
- ClinicalTrials.gov ID
- NCT05836727
- Acronym / sponsor ID
- PELVICOELIO / 29BRC23.0010 - PELVICOELIO
- Conditions
- Pelvic Fracture
- Keywords
- Pelvic ring surgery, Trauma Surgery, Plate Fixation, Laparoscopy, Case series
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 14 participants (estimated)
- Lead sponsor
- University Hospital, BrestUniversity, hospital or other
- Study start
- 1 Mar 2023 (actual)
- Primary completion
- 1 Apr 2023 (actual)
- Study completion
- 1 Jun 2023 (estimated)
- First posted
- 1 May 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Case series to describe the use of laparoscopy for the treatment of pelvic ring disruption.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
Who may qualify
- Ages
- 18 to 100 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- patients who underwent laparoscopy for the treatment of pelvic ring disruption
Key inclusion criteria (1 listed)
- patients who underwent laparoscopy for the treatment of pelvic ring disruption
Key exclusion criteria (1 listed)
- patient < 18 years old
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
conversion rate to open surgery
Time frame: intraoperative
conversion rate to open surgery
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 May 2023.
- Individual participant dataSharing planned: Yes. All collected data that underlie results in a publication
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Pelvic Fracture, run by University Hospital, Brest at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 1 May 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
conversion rate to open surgery (time frame: intraoperative). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 May 2023.