Clinical Analgesic Management in Dementia

NCT07323914 | Recruiting Phase 3

• 1 other identifier: 2025005001
• Study Type: interventional
• Target: 10
• Locations: 1 country
• Sites: 1

Brief Summary

This study is designed to assess the efficacy and safety of oxycodone in managing moderate to severe pain in patients with Alzheimer's disease. The trial will be conducted at Xuanwu Hospital, Capital Medical University, and will enroll 10 eligible participants. Participants will receive oxycodone/acetaminophen (5 mg/325 mg) once daily for 12 weeks. The treatment will follow international guidelines, with dosages adjusted based on the patient's baseline pain levels and individual needs. Dosages will be adjusted based on baseline pain levels and patient needs, following international guidelines. Efficacy and adverse events will be assessed at baseline, week 6, week 12, and at a 12-week post-treatment follow-up. The primary outcome is change in VAS pain scores; secondary outcomes include PAINAD, SF-36, functional ability, and safety profiles.

Conditions

Alzheimer Disease

Keywords

Alzheimer disease; chronic pain; opioid drugs

Outcome Measures

Primary Outcomes (1)

• Pain Assessment in Advanced Dementia Scale (PAINAD)

  baseline, 6 weeks, 12 weeks, 24 weeks.

Secondary Outcomes (8)

• Changes from baseline of exploratory blood biomarkers

  baseline; 12 weeks.

• Mobilization-Observation-Behavior-Intensity-Dementia Pain Scale, version 2 (MOBID-2)

  baseline, 6 weeks, 12 weeks, 24 weeks.

• Change from Baseline in Brain Amyloid Plaque Deposition as measured by PET Scan

  baseline; 12 weeks.

• Change from baseline on the Neuropaychiatic Inventory (NPI)

  baseline; 6 weeks; 12 weeks; 24 weeks.

• Change from baseline on the Alzheimer's Disease Cooperative study-Activities of Daily Living Scale(ADCS-ADL)

  baseline; 6 weeks; 12 weeks; 24 weeks.

Study Arms (1)

Tylex group

EXPERIMENTAL

Drug: Tylex

Interventions

Tylex DRUG

Tylenol (compound oxycodone/acetaminophen) is a non-narcotic analgesic that combines a lower dose of oxycodone (5 mg) with acetaminophen (325 mg). Compared to OxyContin, it provides milder opioid potency and utilizes a synergistic mechanism to achieve pain control with reduced risk of opioid-related side effects.

Tylex group

Eligibility Criteria

• Age: 50 Years - 90 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female, aged 50 to 90 years at the time of enrollment.
• Meets the NIA-AA core clinical diagnostic criteria for probable Alzheimer's disease.
• Clinical Dementia Rating - Global Score (CDR-GS) between 0.5 and 2.0, inclusive, and Clinical Dementia Rating - Memory Box (CDR-MB) score ≥ 0.5.
• Diagnosed with chronic pain within 6 months prior to enrollment and considered appropriate for opioid therapy.
• Presence and severity of pain confirmed using PAINAD, MOBID-2, or comparable scales.
• Educational attainment: at least 4-6 years of formal education, or not illiterate.
• If currently receiving psychotropic or cognitive-enhancing medications, the dosage must have been stable for at least 3 months prior to study entry and remain unchanged during the study. Unless otherwise specified, all other permitted concomitant medications (non-AD related) must be stably administered for at least 4 weeks prior to baseline.
• Has a reliable caregiver/companion who can assist with study participation, defined as a person who can support the participant throughout the study and spend at least 8 hours per week with the participant.
• Willing and able to participate in this clinical trial, to maintain the assigned intervention during the study period, and has signed the informed consent form.

You may not qualify if:

• History of transient ischemic attack (TIA), stroke, or seizure within the past 12 months.
• Presence of any psychiatric diagnosis or symptoms that may interfere with study participation (e.g., hallucinations, major depression, or delusions).
• Known allergy to opioid analgesics.
• Severe visual or hearing impairment.
• Alcohol dependence, substance abuse, or other drug addiction or addictive tendency.
• Current participation in another study related to the treatment of Alzheimer's disease.
• Any other uncontrolled or inadequately treated medical condition (e.g., cardiac, respiratory, gastrointestinal, hepatic, or renal disease), or any condition judged by the investigator to compromise participant safety or interfere with study assessments.
• Any other reason deemed by the investigator to preclude participation in the study.

Sponsors & Collaborators

• Xuanwu Hospital, Beijing: lead

Study Sites (1)

Xuanwu Hospital, Capital Medical University

Beijing, China

RECRUITING

MeSH Terms

Conditions

Alzheimer Disease; Chronic Pain

Condition Hierarchy (Ancestors)

Dementia; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Tauopathies; Neurodegenerative Diseases; Neurocognitive Disorders; Mental Disorders; Pain; Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Officials

• Yi Tang

  M.D., Ph.D.

  STUDY CHAIR

Central Study Contacts

Yi Tang, M.D., Ph.D.

CONTACT

00861083199456; tangyi@xwhosp.org

Ouyang Chen, Ph.D.

CONTACT

15652888562; chenouyang@xwhosp.org

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 23, 2025
• First Posted: January 7, 2026
• Study Start: March 1, 2025
• Primary Completion (Estimated): January 1, 2027
• Study Completion (Estimated): March 31, 2027
• Last Updated: January 7, 2026

Record last verified: 2025-01

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)