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The Effect of Perioperative Hydrogen Inhalation on Post-operative Pain and Inflammation Cytokines

Primary Purpose

Pain, Acute

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
hydrogen inhalation, 4% concentration, given via nasal cannula
Sponsored by
Fu Jen Catholic University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pain, Acute focused on measuring pain, hydrogen inhalation, discectomy

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patient with herniated disc leading to severe neuropathic pain refractory to conservative treatment, receiving endoscopic discectomy.

Exclusion Criteria:

  • American Society of Anesthesiologists class IV or above
  • Sever impairment of heart, lung, kidney and liver and autoimmune disease
  • Less than 20 years old or older than 75 years old
  • Patient refusal
  • Severe complication occurring perioperatively
  • Current pregnancy
  • Hemoglobin less than 10g/dL.

Sites / Locations

  • Fu Jen Catholic University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Hydrogen inhalation group

Traditional care group

Arm Description

Patients allocating to this group received hydrogen inhalation (4% hydrogen given via nasal cannula) with other normal intraoperative care throughout the whole procedure.

Patients allocating to this group received traditional intraoperative care.

Outcomes

Primary Outcome Measures

Post-operative pain
Post-operative pain, measured in visual analogue scale (VAS)
Post-operative pain
Post-operative pain, measured in visual analogue scale (VAS)
Post-operative pain
Post-operative pain, measured in visual analogue scale (VAS)
Post-operative pain
Post-operative pain, measured in visual analogue scale (VAS)
Post-operative pain
Post-operative pain, measured in visual analogue scale (VAS)

Secondary Outcome Measures

Inflammation marker
Inflammation marker, IL-6, IL-10, TNF-alpha

Full Information

First Posted
October 27, 2021
Last Updated
July 25, 2022
Sponsor
Fu Jen Catholic University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05476575
Brief Title
The Effect of Perioperative Hydrogen Inhalation on Post-operative Pain and Inflammation Cytokines
Official Title
The Effect of Perioperative Hydrogen Inhalation on Post-operative Pain and Inflammation Cytokines
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 28, 2021 (Actual)
Primary Completion Date
October 28, 2022 (Anticipated)
Study Completion Date
October 28, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fu Jen Catholic University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To understand the impact of perioperative hydrogen inhalation on post-operative pain control and serum inflammation markers
Detailed Description
Hydrogen is odorless, colorless gas existing in natural environment. It was traditionally thought as biologically inert gas, which means it does not participate in biological process. However, recent studies have demonstrated that ingestion of hydrogen have exerted therapeutic effect on skin squamous cell carcinoma and parasitic hepatitis. Ingestion of hydrogen could also attenuate ischemic-reperfusion injury after stroke by removing reactive oxygen species (ROS). Multiple studies also demonstrated that ingestion of hydrogen exhibit anti-inflammatory effect, leading to less post-operative cognitive impairment, lung graft injury in brain-dead mice and acute lung injury. Means of hydrogen ingestion include oral, inhalation or intravenous injection. Inhalation through simple mask, nasal cannula or ventilator is most convenient way. It has been proved that low concentration of hydrogen inhalation (1%-4%) is effective and safe without causing adverse effects on hemodynamic, respiration or even data of arterial blood gas analysis. High concentration of hydrogen inhalation is proven to be harmless and is often used in diving, treating decompression sickness and preventing arterio-venous thromboembolism. Current data suggests that microglial cells in dorsal root ganglion are activated by danger-associated molecular pattern (DAMP) through toll-like receptor response (TLR) after external insults. Lipopolysaccharides (LPS) are recognized as TLR-4 receptor agonist and data revealed that LPS is associated with significant neuroinflammation and chronic pain process. Peripheral blood monocyte cells(PBSC) could have pro- (e.g. Tumor necrosis factor-α(TNF-α)、Interleukin-6(IL-6)、Interferon-γ(INF-γ) ) and anti- inflammation (e.g. IL-4、IL-5、IL-9、IL-10) cytokines release after LPS stimulation. Current data suggests that hydrogen-rich water ingestion could reduce inflammation and pain score in animal model. Hydrogen inhalation is associated with decrease of pro-inflammation cytokines, such as IL-1β, IL-6, TNF-α and INF-γ. Besides, hydrogen inhalation could lead to reduction of pain in rats with high level spinal cord injury. In addition to observing the difference of pain score between groups, we could also observe the differences between pro- and anti- inflammation cytokines in PBSC after LPS stimulation in patients receiving or not receiving hydrogen inhalation. This could tell us whether the inflammation process is inhibited in cellular level by hydrogen inhalation. To our knowledge, there is no human clinical trials discussing the effect of hydrogen inhalation on chronic pain. We hope to understand the actual impact of hydrogen inhalation on post-operative pain score and inflammation. Further larger scale randomized clinical trials could be carried on based on this result.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Acute
Keywords
pain, hydrogen inhalation, discectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective case control study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
32 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hydrogen inhalation group
Arm Type
Experimental
Arm Description
Patients allocating to this group received hydrogen inhalation (4% hydrogen given via nasal cannula) with other normal intraoperative care throughout the whole procedure.
Arm Title
Traditional care group
Arm Type
No Intervention
Arm Description
Patients allocating to this group received traditional intraoperative care.
Intervention Type
Other
Intervention Name(s)
hydrogen inhalation, 4% concentration, given via nasal cannula
Intervention Description
4% hydrogen inhalation via nasal cannula perioperatively
Primary Outcome Measure Information:
Title
Post-operative pain
Description
Post-operative pain, measured in visual analogue scale (VAS)
Time Frame
immediately post-operative compared to pre-operative pain score measured in VAS
Title
Post-operative pain
Description
Post-operative pain, measured in visual analogue scale (VAS)
Time Frame
12 hours after operation compared to pre-operative pain score measured in VAS
Title
Post-operative pain
Description
Post-operative pain, measured in visual analogue scale (VAS)
Time Frame
24 hours after operation compared to pre-operative pain score measured in VAS
Title
Post-operative pain
Description
Post-operative pain, measured in visual analogue scale (VAS)
Time Frame
1 week after operation compared to pre-operative pain score measured in VAS
Title
Post-operative pain
Description
Post-operative pain, measured in visual analogue scale (VAS)
Time Frame
1 month after operation compared to pre-operative pain score measured in VAS
Secondary Outcome Measure Information:
Title
Inflammation marker
Description
Inflammation marker, IL-6, IL-10, TNF-alpha
Time Frame
immediate post-operation compared to pre-operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patient with herniated disc leading to severe neuropathic pain refractory to conservative treatment, receiving endoscopic discectomy. Exclusion Criteria: American Society of Anesthesiologists class IV or above Sever impairment of heart, lung, kidney and liver and autoimmune disease Less than 20 years old or older than 75 years old Patient refusal Severe complication occurring perioperatively Current pregnancy Hemoglobin less than 10g/dL.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chao Hsien Sung, MD
Phone
+886-912072103
Email
joe411002@gmail.com
Facility Information:
Facility Name
Fu Jen Catholic University Hospital
City
New Taipei City
ZIP/Postal Code
24300
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sung Chao Hsien, MD
Phone
0912072103
Email
joe411002@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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The Effect of Perioperative Hydrogen Inhalation on Post-operative Pain and Inflammation Cytokines

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