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Pain Control clinical trials

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NCT ID: NCT04995497 Completed - Clinical trials for Erector Spinae Plane Block

Intravenous(IV) vs. Erector Spinae Plane Blocks in Cardiac Surgery

Start date: August 15, 2021
Phase: Phase 2
Study type: Interventional

Interfascial plane blocks have been developed for analgesia, among which the erector spinae plane (ESP) has gained popularity. The ESP block has been hypothesized to provide truncal analgesia by spread of local anesthetic into the paravertebral space. Recent studies have contested this idea showing unreliability in the spread of the local anesthetic into the paravertebral space.

NCT ID: NCT04292171 Completed - Pain Control Clinical Trials

Gabapentin for Perioperative Pain Relief in Surgical Abortion

Start date: May 1, 2017
Phase: Early Phase 1
Study type: Interventional

Gabapentin preoperative use for evaluation of benefit to reduce pain during and after surgical office-based abortion.

NCT ID: NCT03921190 Completed - Anesthesia, Local Clinical Trials

Should Maxillary Buccal Infiltration Anesthesia be Given in a Closed Mouth Technique?

Start date: April 29, 2019
Phase: N/A
Study type: Interventional

To study the patients' and dentists' perception of receiving/ administering maxillary buccal infiltration anesthesia using an open or closed mouth techniques

NCT ID: NCT03840356 Completed - Pain Clinical Trials

Postoperative Pain Reported to Nurses and Physicians

Start date: June 18, 2018
Phase:
Study type: Observational

Effective pain control following surgical procedures is a goal for both the patient as well as the medical staff caring for them. There have been numerous studies evaluating differing treatment pathways, but most studies have relied on the Visual Analog Scale (VAS) or Numerical Rating Scale (NRS) to evaluate outcomes. These scales are subjective score given by the patient with no objective data input, therefore making comparisons subject to possible bias. There are no known studies comparing the pain scores provided by the patient to the surgical team compared to the nursing staff caring for the patient. The aim will be to compare these values to see if patients are consistent in their pain rating.

NCT ID: NCT03493828 Completed - Pain Control Clinical Trials

Efficacy of TAP Block in Cesarean Section Patients

Start date: June 2013
Phase: Phase 3
Study type: Interventional

TAP Block done with 2 different concentrations of bupivacaine and placebo

NCT ID: NCT03024515 Completed - Pain Control Clinical Trials

Opioids Titration Study in Advanced Cancer Patients in Hong Kong

Start date: August 23, 2018
Phase: N/A
Study type: Interventional

Pain is a common symptom that is experienced by patients with advanced cancer. Whilst mild pain can usually be controlled with simple analgesics, more severe pain may require initiation of opioid analgesics. The World Health Organization (WHO) has developed a specific guideline for titration of analgesics. Known as the WHO Pain Ladder, patients who have severe pain despite non-opioid and weak opioid analgesics are advised to step up to level 3 - "Strong Opioids". Morphine is the most common opioid strong analgesic prescribed in Hong Kong. To the best of our knowledge, there is no formal opioid pain control guideline developed for cancer patients in Hong Kong. The prescription practices of various physicians who treat advance cancer patients, including oncologists and palliative care physicians have never been audited or standardized. Furthermore, there are inherent issues with the administration of oral morphine. Currently, only one fixed concentration is available in a liquid formulation. Patients are known to have difficulties in receiving the appropriate dose. Accurate measurement of the volume required is extremely difficult, and many a times patients will report to have spilled the oral morphine during decanting, or will report that they have not been taking adequate doses because they are worried that they will decant too much into a spoon or syringe and overdose themselves. Oxycodone is a semisynthetic strong opioid analgesic, which has recently been introduced to Hong Kong. It is formulated as a capsule, and again, 2 preparations (sustained-release (Oxycontin) and immediate release (Oxycodone IR)) are available. Inherent advantages include ease of administration; different groups have previously reported less adverse effects and better treatment compliance. However, to date, there has been no prospective 'head-to-head' comparison have ever been carried out comparing this with the traditional, well-accepted methods. The purpose of this study is to assess whether or not the use of Oxycontin and Oxycodone IR may be superior to traditional medication choices and schedules in terms of time required for onset of pain control, the side effect profile, patients' tolerability and compliance to treatment. Interestingly, through this randomized open-label prospective study, we also aim to capture information on current opioid prescription practices by clinicians who manage patients with advanced cancers, which will be useful for us to consider the establishment of territory-wide treatment guidelines at a later juncture.

NCT ID: NCT01578174 Completed - Pain Control Clinical Trials

The Effect of Dexmedetomidine in the Management of Pain After Uterine Artery Embolization

Start date: April 2012
Phase: N/A
Study type: Interventional

The investigators examined the effect of dexmedetomidine in the management of pain after uterine artery embolization.

NCT ID: NCT01226186 Completed - Pain Control Clinical Trials

Self Medication With Oral Morphine After Total Knee Arthroplasty.

Start date: October 2010
Phase: N/A
Study type: Interventional

The study aims to compare two post operative pain management strategy's, traditional nurse dispensed pain control versus patient self medication. The investigators aim to establish if patients who self medicate have differing pain levels than those who take nurse dispensed oral morphine.

NCT ID: NCT00970112 Completed - Pain Control Clinical Trials

Dexamethasone and Etoricoxib for Pain Prevention Following Periodontal Surgery

Start date: November 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to investigate whether preemptive medication with dexamethasone or etoricoxib provides better pain management and control than placebo following periodontal surgery.