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AzTrials

Condition

Analgesia Clinical Trials

Studies of analgesia, matched by condition name and medical subject headings. Start with those open to enrolment.

1,418 registered studies

In numbers

Open to volunteers
295
Active
328
With results posted
65
All registered
1,418

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 295
  • Laparoscopic Surgery, Visceral Pain, Postoperative

    Anrikefon-based Patient-controlled Intravenous Analgesia Following Laparoscopic Surgery

    • Recruiting
    • Age: 18 to 75 years
    • Phase 4
    • Injection or infusion

    Visceral pain following laparoscopic surgery is frequently underestimated, yet it is associated with a range of adverse outcomes.

    Conditions
    Laparoscopic Surgery, Visceral Pain, Postoperative, Anrikefon, Patient-controlled Intravenous Analgesia
    Trial name
    NCT07525986
    Testing
    High-dose anrikefon, Medium-dose anrikefon, Low-dose anrikefon
    Where
    4 sites in China
    Volunteers
    140 people
    Sponsor
    Peking University First Hospital
    Can I take part? NCT07525986
  • Analgesia

    Evaluation of Three Different Antalgic Blocks in Total Knee Prosthesis

    • Recruiting
    • Age: 40 years and older
    • Injection or infusion

    This randomised trial examines the three main anaesthetic blocks used in knee replacement surgery, comparing them in terms of analgesic efficacy (primary outcome), range of motion and degree of flexion in the immediate…

    Trial name
    Analgesia PTG (NCT07751653)
    Testing
    Levobupivacaine
    Where
    2 sites in Italy
    Volunteers
    142 people
    Sponsor
    I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
  • Abnormal Uterine Bleeding, Analgesia

    Combined Ketorolac and Lidocaine Paracervical Block for Office Hysteroscopy

    • Enrolling by invitation
    • Age: 18 years and older
    • Phase 1
    • Surgery or procedure

    A randomized double-blind placebo controlled trial comparing the effect of a combined ketorolac and lidocaine paracervical block with a standard lidocaine paracervical block on procedure related pain with office hysteroscopies.

    Conditions
    Abnormal Uterine Bleeding, Analgesia, Paracervical Block
    Trial name
    NCT06653400
    Testing
    paracervical block, Lidocaine, ketorolac
    Where
    United States
    Volunteers
    60 people, healthy volunteers welcome
    Sponsor
    Icahn School of Medicine at Mount Sinai
    Can I take part? NCT06653400
  • Cesarean Section (MeSH: D002585), Anesthesia

    Evaluation of Consciousness Depth (qCON) and Analgesia Depth (qNOX) Indices in General Anesthesia

    • Not yet recruiting
    • Age: 18 to 45 years
    • Observational study

    Objective: This prospective, single-center, observational clinical study aims to evaluate changes in qCON (hypnotic depth), qNOX (nociception/analgesia depth), EMG, and other parameters in patients undergoing elective cesarean…

    Conditions
    Cesarean Section (MeSH: D002585), Anesthesia, Intraoperative Awareness, Analgesia
    Trial name
    NCT07887919
    Volunteers
    140 people, healthy volunteers welcome
    Sponsor
    Kudret Dogru
    Can I take part? NCT07887919
  • Cancer, Palliative Care, Patient Care

    Dexmedetomidine for Refractory Pain in Palliative Cancer Patients

    • Recruiting
    • Age: 18 years and older
    • Observational study

    The goal of this study is to find out whether the medication dexmedetomidine can be a safe and effective additional treatment for cancer patients whose pain is not well controlled by standard pain medicines (such as opioids).

    Conditions
    Cancer, Palliative Care, Patient Care, Pain Management, Dexmedetomidine Analgesia
    Trial name
    DEX-PAL (NCT07885475)
    Where
    4 sites in Norway
    Volunteers
    30 people
    Sponsor
    St. Olavs Hospital
    Can I take part? DEX-PAL
  • Sedation, Analgesia Assessment

    A Prospective Multicenter Registry Study of Sedation and Analgesia in Critically Ill Patients

    • Enrolling by invitation
    • Age: 18 years and older
    • Observational study

    Sedation and analgesia are essential components of comprehensive care for intensive care unit (ICU) patients, particularly those receiving invasive mechanical ventilation, undergoing invasive procedures, or experiencing pain…

    Conditions
    Sedation, Analgesia Assessment, ICU
    Trial name
    NCT07885930
    Testing
    Not applicable- observational study
    Where
    China
    Volunteers
    2,000 people
    Sponsor
    Beijing Chao Yang Hospital
    Can I take part? NCT07885930
  • Pain, Analgesia

    Impact of the NeuroCuple Device on Pain Management After Cesarean Delivery

    • Recruiting
    • Age: 18 years and older
    • Medical device

    This will be a single-center, sham-controlled, 3 arms, randomized (1:1:1) prospective study in females undergoing cesarean delivery to investigate the impact of NeuroCuple™ non-pharmacological analgesic device for management of…

    Conditions
    Pain, Analgesia, Pregnancy
    Trial name
    NCT07185425
    Testing
    NeuroCuple
    Where
    United States
    Volunteers
    180 people
    Sponsor
    Inova Health Care Services
    Can I take part? NCT07185425
  • Labor Analgesia, Labor Pain

    Effect of Dural Puncture Epidural Analgesia on Oxytocin in Early vs Late Labor

    • Not yet recruiting
    • Age: 18 to 40 years
    • Observational study
    • Injection or infusion
    • Surgery or procedure

    Oxytocin is a key hormone that regulates uterine contractions during labor. Dural Puncture Epidural Analgesia (DPEA) is a modern technique for labor pain relief that provides faster onset and more reliable analgesia than standard…

    Conditions
    Labor Analgesia, Labor Pain, Oxytocin
    Trial name
    DPEA-OXY (NCT07873814)
    Testing
    Dural Puncture Epidural Analgesia (DPEA)
    Where
    Turkey (Türkiye)
    Volunteers
    120 people
    Sponsor
    Ankara City Hospital Bilkent
    Can I take part? DPEA-OXY
  • Postoperative Analgesia in Patients Undergoing Open Renal Surgery

    Ultrasound-Guided Midpoint Transverse Process to Pleura Block Versus Erector Spinae Plane Block for Postoperative Analgesia in Patients Undergoing Open Renal Surgery :A Randomized Comparative Study.

    • Not yet recruiting
    • Age: 18 to 65 years
    • Surgery or procedure

    The goal of this randomized comparative clinical trial is to compare the analgesic effectiveness of ultrasound-guided Midpoint Transverse Process to Pleura (MTP) block versus Erector Spinae Plane (ESP) block in adult patients…

    Trial name
    NCT07881523
    Testing
    Midpoint Transverse Process to Pleura (MTP)Block, Erector spinae plane (ESP) block
    Where
    Egypt
    Volunteers
    50 people
    Sponsor
    Minia University
    Can I take part? NCT07881523
  • Placebo Analgesia, Pediatric Pain

    Applying a Small Procedure Prior to Injection/Vaccination Reduces Pain in Children

    • Not yet recruiting
    • Age: 6 to 14 years
    • Vaccines
    • Injection or infusion

    In this proposed study, the investigators aim to apply a minor procedure prior to a treatment that induces pain (e.g., injection/vaccination) to help manage pediatric pain.

    Conditions
    Placebo Analgesia, Pediatric Pain, Vaccination
    Trial name
    NCT06313788
    Volunteers
    180 people, healthy volunteers welcome
    Sponsor
    Lingnan University
    Can I take part? NCT06313788

Completed, with results posted

All –
  • Post Operative Analgesia, Bariatric Surgery

    Oral Acetaminophen for Post-Op Pain Management in Bariatric Surgery Patients

    • Completed
    • Age: 18 years and older
    • Phase 2
    • Pill or oral medicine
    • Results posted

    Adult patients with morbid obesity who have had Roux-en-Y gastric bypass (RYGB) or laparoscopic sleeve gastrectomy (LSG) surgery have impaired drug metabolism.

    Conditions
    Post Operative Analgesia, Bariatric Surgery, Bariatric Surgery (Gastric Bypass), Bariatric Surgery Patients
    Trial name
    NCT06658574
    Testing
    Acetaminophen
    Where
    United States
    Volunteers
    65 people
    Sponsor
    Rutgers, The State University of New Jersey
    Can I take part? NCT06658574
  • Labor Pain, Analgesia

    Optimal Bupivacaine Dose for Initiation of Labor Epidural Techniques

    • Completed
    • Age: 18 to 50 years
    • Phase 4
    • Results posted

    To estimate the dose of bupivacaine required to achieve initial effective comfort in 90% of patients (ED90) via the epidural (DPE or EPL) technique in women undergoing labor.

    Trial name
    NCT04814537
    Testing
    Bupivacaine Hydrochloride
    Where
    United States
    Volunteers
    100 people, healthy volunteers welcome
    Sponsor
    Brigham and Women's Hospital
  • Analgesia

    HTX-011 for Post-bunionectomy Analgesia

    • Completed
    • Age: 18 to 65 years
    • Phase 2
    • Results posted

    A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Two-Part Evaluation of the Efficacy and Safety of Locally Administered HTX-011 for Postoperative Analgesia Following Bunionectomy

    Trial name
    HTX-011 (NCT02471898)
    Testing
    HTX-011
    Where
    United States
    Volunteers
    71 people
    Sponsor
    Heron Therapeutics
    Can I take part? HTX-011
  • Head and Neck Cancer, Analgesia

    Multimodal Pain Study in Free Flap Patients

    • Completed
    • Age: 18 years and older
    • Phase 4
    • Injection or infusion
    • Results posted

    This study will be a randomized, prospective study comparing Pain Management Arm A and Pain Management Arm B. Arm A will have scheduled Tylenol with opioids available as needed (PRN) in the peri-operative period.

    Trial name
    NCT04246697
    Testing
    Tylenol, Oxycodone, Morphine
    Where
    United States
    Volunteers
    30 people
    Sponsor
    University of Kansas Medical Center
  • Analgesia

    Study of Post-Herniorrhaphy Non-opioid MMA Regimens

    • Completed
    • Age: 18 years and older
    • Phase 3
    • Medical device
    • Results posted

    This is a Phase 3b, open-label study to assess postoperative opioid use in subjects undergoing unilateral open inguinal herniorrhaphy with intraoperative administration of HTX-011 and a postoperative non-opioid multimodal…

    Trial name
    NCT03907176
    Testing
    HTX-011, Luer lock applicator, Ibuprofen
    Where
    30 sites in United States
    Volunteers
    209 people
    Sponsor
    Heron Therapeutics

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