Study to Evaluate a Preop Dose of Brivoligide Injection for Pain After Knee Replacement in Patients With High PCS Scores

Pain, Postoperative Clinical Trial

Official title:

A Phase 2 Randomized Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of a Single Intrathecal Preoperative Administration of Brivoligide Injection in Patients With a Pain Catastrophizing Scale Score ≥16 Undergoing Unilateral Total Knee Arthroplasty

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT03797612
• Other study ID #: ADYX-005
• Status: Withdrawn
• Phase: Phase 2
• Start date: January 2021
• Est. completion date: February 2022

Study information

• Verified date: July 2020
• Source: Adynxx, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multi-center, Phase 2, randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of brivoligide injection administered intrathecally before surgery in patients with a Pain Catastrophizing Scale (PCS) score ≥16 undergoing primary unilateral total knee arthroplasty.

Description:

The objective of this study is to evaluate the safety and postoperative pain reducing efficacy of a single preoperative intrathecal administration of brivoligide injection in patients with a Pain Catastrophizing Scale (PCS) score ≥16 undergoing unilateral total knee arthroplasty.

Potential subjects will be prescreened for PCS scores of 16 or greater in advance; pre-qualified patients will be invited to the investigative site for informed consent and full screening within 30 days of randomization. Patients providing informed consent and meeting all study eligibility criteria will be enrolled in the study on the day of surgery (Day 1). Safety assessments will be performed through Day 28; efficacy assessments will be conducted at the follow-up visits and daily via electronic diary by subjects through Day 42. Follow up visits will occur on Days 7, 14, 21, 28, and 42.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: February 2022
• Est. primary completion date: January 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years and older

Eligibility

Inclusion Criteria:

• Score of 16 or greater on the PCS scale

• Scheduled for primary unilateral TKA with spinal anesthesia as the primary anesthetic for painful osteoarthritis without congenital knee pathology

• American Society of Anesthesiologists Physical Status Classification System = 3

• Medically stable for elective surgery with spinal anesthetic as determined by the Investigator

• Body mass index of 18-45 kg/m2

• Stable medical regimen at least 1 week before randomization

• Able to read and understand study instructions in English or Spanish, and willing to comply with all study procedures

Exclusion Criteria:

• Target knee > 20 degrees valgus or varus deformity, evidence of significant bone loss or ligamentous laxity, or existing major hardware that requires removal during TKA

• Inflammatory arthridities (e.g., rheumatoid arthritis, lupus, ankylosing spondylitis, psoriatic arthritis), with the exception of clinically stable/non-active gout

• Undergoing concomitant surgical procedures or non-elective TKA, or contralateral knee is likely to require TKA within 6 weeks (or would interfere with study assessments)

• Use of cryoneurolysis (including Iovera) on the current operative knee region within 6 months prior to randomization and/or at any time through the duration of the study

• Planned use of general anesthesia as the primary anesthetic; planned use of neuroaxial (intrathecal or epidural) opioids, or any use of extended release/long acting opioids or ketamine preoperatively and/or at any time through the duration of the study

• Use of more than 40 mg per day (on average) of oral morphine or its equivalent within 1 month prior to randomization

• Current neurologic disorder, which could confound the assessment of pain (e.g., Parkinson's, Multiple Sclerosis)

• Unstable mental condition and/or evidence of an uncooperative attitude in the opinion of the Investigator; subjects diagnosed with schizophrenia, prescribed antipsychotic medications or MAOIs

• Women who are pregnant or nursing

• Subjects engaged in pending or active litigation, or seeking disability compensation; subjects whose cases have been settled or finally decided are not excluded

• Participation in a clinical trial with the last dose or intervention within 1 month of randomization, or planned participation in a clinical trial during this study

• Previous participation in any study involving brivoligide injection

Related Conditions & MeSH terms

• Pain, Postoperative

Intervention

Drug:
• Brivoligide Injection 660 mg/6 mL
Single preoperative intrathecal injection
• Placebo 6 mL
Single preoperative intrathecal injection

Locations

Country	Name	City	State
United States	Research Site	Phoenix	Arizona
United States	Research Site	Sheffield	Alabama

Sponsors (1)

Lead Sponsor	Collaborator
Adynxx, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Numerical Rating Scale (NRS) Pain with Walking 15 Meters	Least squares mean pain rating (NRS) with walking during the 15-meter walk Day 7 to Day 28	Day 7 to Day 28
Secondary	Numerical Rating Scale (NRS) Pain at Rest	Least squares mean pain rating (NRS) at rest Day 7 to Day 28	Day 7 to Day 28
Secondary	Numerical Rating Scale (NRS) Pain with 90 Degrees Passive Knee Flexion	Least squares mean pain rating (NRS) with passive knee flexion to 90 degrees from Day 7 to Day 28	Day 7 to Day 28
Secondary	Total Postoperative Opioid Use	Total use of postoperative opioid medications (morphine equivalents) to Day 42	Postoperative through Day 42
Secondary	Time to Numerical Rating Scale (NRS) Pain = 3 for Worst Pain	Time to achieve NRS pain score = 3 for worst pain	Postoperative through Day 42