ID
Bron
Aandoening
Total knee arthroplasty, persisting pain, chronic pain
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
- Persistent postsurgical pain (PPSP)<br>
- eQST<br>
o Electrical pain threshold (ePT) [mA]<br>
o Electrical pain tolerance threshold (ePTT) [mA]<br>
- Nociceptive Perception thresholds (NPT)<br>
o Stimulus amplitude [mA]<br>
o Responses to stimuli (perceived/not perceived)<br>
o Stimulation time [s]<br>
Achtergrond van het onderzoek
Background of the study:
Total knee arthroplasty (TKA) often produce severe persistent postsurgical
pain (PPSP), and in some cases, chronic pain. While the acute pain postpones the early recovery, the chronic pain seriously restricts an individual’s quality of life, and also increases costs of global health care and absenteeism at work. Central sensitization plays a major role in the development of PPSP. Sensitization is characterized by generalized hyperalgesia and can be detected by means of a decrease in (electrical) pain threshold. Recently, a pilot study showed that presurgical electrical pain tolerance thresholds (ePTT) have predictive value for PPSP in abdominal surgery patients. Other pilot studies suggest that, in addition to ePTTs, electrical nociceptive perception thresholds (eNPTs), when tracked over a short period of time (e.g. 25 minutes) can be expected to be able to observe changes in peripheral and/or central mechanisms in more detail than regular EPTs. Results after TKA show similar persisting pain incidences as after abdominal surgery. Therefore, these patients are a suitable population to study the generalizability of the results found in previous studies.
Objective of the study:
The main objective of this study is to investigate the predictability of persisting postsurgical pain (PPSP) after TKA using electrical quantitative sensory testing (eQST) and nociceptive perception thresholds (NPT) in combination with a presurgical conditioning pain modulation (CPM) paradigm. The secondary objectives of this study are to investigate (1) the effect of TKA on stimulus specific changes in NPT, and (2) the correlation between eQST versus NPT and PPSP.
Study design:
Monocentre prospective observational study
Onderzoeksopzet
Preoperative: baseline measurement at -35 to -7 days
Postoperative: days 2, 42, 84, 168, and 365
Onderzoeksproduct en/of interventie
Not applicable
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Patients scheduled for total knee arthroplasty.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Patient’s refusal
- Preexisting neurological or psychiatric illnesses
- Chronic pain syndromes
- Alcohol or drug abuse
- Suspected possibility of delirium
- Difficulties in communication
- Rheumatoid arthritis
- Revision knee surgery or participation in another study
- Presurgicaloperative ASA score >3
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL4710 |
NTR-old | NTR4981 |
CCMO | NL47455.091.14 |
OMON | NL-OMON40450 |