Chronic Postsurgical PainPOCSENCT06555107
Acute Preoperative Pain and Chronic Post-surgical Pain in Emergency Surgery
A study testing questionnaire and phone call in people with Chronic Postsurgical Pain and Acute Pain, run by Centre Hospitalier Universitaire, Amiens at 1 site in France.
Trial summary
Studies evaluating postoperative pain as a risk factor for CPSP are almost exclusively carried out in the context of scheduled surgery. As a result, the preoperative pain studied as a risk factor for chronicity is essentially a state of pain that has persisted for several weeks or even several months. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Postsurgical Pain, Acute Pain, Emergency Surgery
- What is being tested?
- questionnaire and phone call
- How many people
- 693 participants
- Where
- 1 siteFrance
- Study dates
- 29 Aug 2024to Apr 2027
- Phase
- Interventional
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 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age ≥18 years old.
- Emergency orthopaedic and/or abdominal surgery.
- Informed consent.
- Affiliation to a social security scheme
Who cannot join
- Intraoperative complications that are life-threatening or require the surgical procedure to be discontinued.
- Post-operative intensive care unit admission.
- Ambulatory surgery.
- Endoscopic surgery.
- Repeat surgery at the same site in less that 3months.
- Pregnant or breast-feeding patients.
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- Patients under guardianship or deprived of liberty.
- Patients suffering from psychiatric pathologies.
- Patients suffering from neurodegenerative pathologies.
- Patients for whom self-assessment of pain using a numerical scale (0-10) cannot be carried out (non-communicative patients, non-French-speaking patients, and so on).
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
France1 site, 1 recruiting
- Recruiting
CHU Amiens-Picardie
Amiens, 80054
Paul TARPIN, MD, 0322087980, Tarpin.Paul@chu-amiens.fr
Ottilie Fumery, MD
About this study
Studies evaluating postoperative pain as a risk factor for CPSP are almost exclusively carried out in the context of scheduled surgery. As a result, the preoperative pain studied as a risk factor for chronicity is essentially a state of pain that has persisted for several weeks or even several months.
In emergency surgeries, patients are subject to acute preoperative pain of varying intensity and the duration of which may vary by a few days. A few studies have highlighted the intensity of acute preoperative pain as a factor favouring moderate to severe postoperative pain. At this point, no study has addressed the long-term consequences of this intense preoperative pain the emergency context.
Read more
An evaluation in the field of emergency surgery, where the preoperative pain is often intense and limited in time, would enable us to identify more precisely the impact of acute pain on the incidence of CPSP.
The investigators are hypothesising that the occurrence of CPSP at 3 months in patients undergoing emergency orthopaedic or abdominal surgery is associated with acute preoperative pain.
- Conditions
- Chronic Postsurgical Pain, Acute Pain, Emergency Surgery, Opioid, Postoperative Pain, Risk Factors
- Being tested
- questionnaire, phone call
- Keywords
- risk factors, Chronic Postsurgical Pain, Acute Pain, emergency surgery, opioid, Postoperative Pain
- Medical subject headings
- Pain, Postoperative, Acute Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
questionnaireOther
Patients included in the study will be asked to complete a questionnaire 48 to 72 hours after surgery to assess their perception of pain and preoperative anxiety
phone callOther
Patients will then be interviewed by phone 3 months after their emergency surgery. During the interview, they will be questioned via a standardised questionnaire on the existence of CPSP
What is being measured
The primary outcome is the main question the study is designed to answer.
Frequency of CPSP
Measured: at 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Aug 2024
- Study start29 Aug 2024
- Primary completionJan 2027 (estimated)
- Study completionApr 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Postsurgical PainStudies of the same condition, open and under way.
- 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 693 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier Universitaire, Amiens
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06555107
- Sponsor's protocol ID
- PI2024_843_0038
- Acronym
- POCSE
- Status last verified
- Jan 2026
- First submitted
- 13 Aug 2024
- Last updated
- 16 Jan 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No