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Peripheral Nerve Block Anaesthesia for Ankle Fracture Surgery - an Exploratory Study: Is Rebound Pain a Problem?

Peripheral Nerve Block Anaesthesia for Ankle Fracture Surgery - an Exploratory Study: Is Rebound Pain a Problem?

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02100098
Enrollment
21
Registered
2014-03-31
Start date
2014-03-31
Completion date
2015-03-31
Last updated
2015-04-20

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

Conditions

Postoperative Pain

Keywords

Ankle fracture, Nerve block, Postoperative pain, Pain profile, Rebound pain

Brief summary

The purpose of this exploratory study is to characterize the postoperative pain profile of patients undergoing operation with internal fixation of an ankle fracture under nerve block anaesthesia. Special attention is payed towards the possible existence and clinical relevance of a rebound pain phenomenon upon cessation of the nerve block. Results are used to guide the set up of a randomized controlled trial on the subject.

Detailed description

Peripheral nerve blocks (PNB) are widely used as anaesthesia and postoperative pain control for surgery. Several studies have suggested multiple benefits of PNB's but primarily shown in elective surgery. Acute conditions like ankle fractures have a different pain profile and risks and benefits of PNB's have not been sufficiently researched in these cases. A recent study (Goldstein et al. 2012) suggested that a rebound pain effect occur upon cessation of PNB effect defined as a pain increase to a significantly higher level than observed in patients with no PNB at the same point after surgery. With this prospective, exploratory study we aim to examine the postoperative pain profile after PNB anaesthesia for ankle fracture surgery with focus on plausibility of a rebound pain effect (as defined above) upon PNB cessation. Secondarily to explore a variety of factors related to postoperative pain profile and feasibility of PNB anaesthesia for ankle surgery including efficacy, risk factors, time factors as well as postoperative recovery and overall patient satisfaction. Results will provide focus for a following randomized controlled trial.

Interventions

None listed

Sponsors

Herlev Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients \>= 18 years old scheduled for internal fixation of an ankle fracture as defined above. * Ability to read and understand Danish and give informed oral and written consent

Exclusion criteria

* Multitrauma patients / other simultaneous fractures * Cognitive or psychiatric dysfunction causing expected inability to comply with study protocol * CAVE nonsteroidal antiinflammatory drugs (NSAID) or Morphine or Local Anaesthetics as evaluated by anesthesiologist for any reason * Primary investigator unavailable for PNB administration at scheduled time of operation * Infection at PNB injection site * Time from fracture to operation \> 5 days * Existing neuropathy with functional impairment of the fractured extremity * Bodyweight \< 50 kg * Daily use of opioids \> 2 weeks preoperatively * Pregnancy * Nephropathy requiring dialysis

Design outcomes

Primary

MeasureTime frameDescription
Clinically relevant pain increase based on analysis of Numeric Rating Scale pain score (NRS) area under the curve (AUC) for the time period 12-24 hours compared to 0-12 hours postoperatively.0, 2, 4, 6, 9, 12, 15, 18, 21 and 24 hours postoperativelyPain scores are assessed and marked by the patient on a 0-10 numeric rating pain scale (NRS).

Secondary

MeasureTime frameDescription
Calculated Composite Score for the time intervals 0-24h, 0-12h and 12-24h postoperatively0-24 hours postoperativelyWe will calculate the Silverman composite score of opioid use and pain score combined. This in order to illustrate any increase in pain and to use for sample size calculations for a future randomised study on the subject.
Time to first opioid dose postoperatively0-24 hours postoperatively
Opioid use 12-24 hours compared to 0-12 hours postoperatively0-24 hours continuous measurementRescue morphine doses are administered intravenously via a patient controlled analgesia (PCA) pump when needed. Times of use are electronically registered.
NRS day 1-7 as both average and worst of the dayDays 1-7 postoperativelyNRS are filled out by the patient in a diary.
Daily opioid consumption day 1-7Days 1-7 postoperativelyRegistered in a diary.
Time to patient estimated cessation of block effect0-24 hours postoperatively

Other

MeasureTime frameDescription
Antiemetic medication 24h postoperatively0-24 hours postoperatively
Time used for PNB administrationPreoperatively
Time to PNB effect on sensory and motor functionPreoperatively
Clinically relevant pain increase based on analysis of Numeric Rating Scale pain score (NRS) area under the curve (AUC) after cessation of nerve block compared to before cessation of nerve block.0, 2, 4, 6, 9, 12, 15, 18, 21 and 24 hours postoperativelyThe average postoperative time to cessation of nerve block defining the time periods for this comparison will be defined after visual evaluation of the given pain profiles.
Duration of surgeryOperation day
Partial block rate and Failed block rateOperation dayPartial = need for supplemental block preoperatively (if PNB seems insufficient after 30 min). Failed = need for General Anaesthesia.
Need for PACU admission postoperativelyOperation dayMost patients are expected to be send directly to the Orthopaedic ward following surgery. If not, the reason is noted.
Length of stay in the Operation Room (OR) - total and pre- and post-operativelyOperation day
Score of the Quality of Recovery-15 (QoR-15) questionnaire preoperatively and on postoperative day 1.Preoperatively and postoperative day 1Validation of the Danish translation of QoR-15 in this population of patients undergoing acute orthopaedic surgery under PNB-anaesthesia. A Danish version of the QoR-15 questionnaire is currently being validated in a mixed surgical patient population receiving surgery under general anaesthesia. We will attempt to validate the questionnaire on patients receiving nerve block (PNB) anaesthesia.
QoR-15 questionnaire score on day 1, 2 and 7 postoperativelyPostoperative day 1, 2 and 7.
Length of postoperative stay in hospitalUp to 3 weeks
Time to first meal/appetite postoperatively0-24 hours postoperatively
Incidence of postoperative nerve symptoms (PONS) on day 7Postoperative day 7Telephone interview
Postoperative nausea and vomiting (PONV) 24 hours postoperatively0-24 hours postoperatively

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026