ClinicalTrials.Veeva

Menu

Longitudinal Assessment of Pain-Related Patient-Reported Outcomes After Surgery

J

Jena University Hospital

Status

Invitation-only

Conditions

Adult
Pain Management
Pain, Postoperative
Pain Measurement
Analgesia
Functional Status
Neuralgia

Study type

Observational

Funder types

Other

Identifiers

NCT05315596
JenaUH_pain

Details and patient eligibility

About

Little is known about pain-related outcomes experienced by patients in the first few weeks after surgery, once they are discharged from hospital.

This study aims to characterize pain, pain-related interference, and early neuropathic pain in the sub-acute phase after surgery.

Full description

A high proportion of patients experience moderate to severe pain after surgery. However, most of the knowledge about this comes from studies where patients are evaluated in the hours and up until the first postoperative day. Alternatively, patients are assessed several months (eg 3 or later) after surgery, to evaluate the development of chronic pain related to surgery (CPSP) and most patients do not develop CPSP.

This study aims to learn how patients recover concerning pain and function once they return home after surgery. How long is it before they can resume their daily activities and to do so in comfort? Do they take treatment for pain? Do they have pain restricted to the surgical incision or it is more widespread? There is little knowledge as to whether there are signs of nerve injury in the days close to surgery. This type of pain might lead to chronic pain in later stages.

Patients will be assessed at three time points: the first day after surgery, the 7th day after surgery, and 1 month.

The information we obtain will offer healthcare providers, from multiple hospitals, information about the care they provide to their patients for pain while patients are still in hospital and insights as to how the care might be improved, once they are discharged.

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Adult
  2. On the first post-operative day and back on the ward for at least 6 hours
  3. Gives consent for assessment at 3-time points

Exclusion criteria

  1. The patient is unable to communicate
  2. The patient is cognitively impaired
  3. The patient is asleep
  4. The patient is too ill or in too much pain and does not wish to be interviewed
  5. The patient does not wish to fill in the outcomes questionnaire

Trial contacts and locations

16

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems