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Trial Title:
Preoperative Oral Midazolam to Postoperative Pain Relief in Sleep Disturbance or Anxiety Patients With Colorectal Cancer
NCT ID:
NCT06407518
Condition:
Preoperative
Sleep Disturbance
Anxiety
Midazolam
Pain, Postoperative
Conditions: Official terms:
Colorectal Neoplasms
Dyssomnias
Parasomnias
Pain, Postoperative
Anxiety Disorders
Midazolam
Pharmaceutical Solutions
Conditions: Keywords:
preoperative
oral midazolam
sleep disturbance
anxiety
postoperative pain
colorectal cancer
Study type:
Interventional
Study phase:
N/A
Overall status:
Not yet recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Prevention
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Intervention:
Intervention type:
Drug
Intervention name:
Midazolam oral solution
Description:
Each individual administers the midazolam oral solution nightly from enrollment to the
surgry.
Arm group label:
Midazolam oral solution Group
Other name:
Midazolam oral solution, YICHANG HUMANWELL PHARMACEUTICAL
Intervention type:
Other
Intervention name:
Placebo
Description:
Each individual administers placebo solution nightly from enrollment to the surgry.
Arm group label:
Control Group
Summary:
Previous studies have indicated a high incidence of sleep disturbances and anxiety
symptoms in individuals with colorectal cancers prior to undergoing surgery, leading to
worsened postoperative pain, slower recovery, and higher risk of chronic pain. The
enhancement of sleep quality is intricately linked to reducing stress. Preoperative drugs
that combine hypnosis and anti-anxiety have not been studied in colorectal cancer
patients. Midazolam oral solution is safe and effective for short-term hypnotic and
anti-anxiety effects in clinical preoperative settings. In the current randomized
controlled clinical trial, 280 patients experiencing sleep disturbance or anxiety prior
to colorectal cancer surgery will receive midazolam solution to assess its potential
efficacy in reducing postoperative pain, expediting recovery, and decreasing the
likelihood of chronic pain. Additionally, the study aims to explore the potential
connections between midazolam administration and reductions in stress and inflammation.
Detailed description:
Preoperative sleep disturbance and anxiety worsen postoperative pain for patients
undergoing surgeries. Research indicates that a significant proportion of patients,
ranging from 8.8% to 79.1%, experience disturbances in sleep or anxiety prior to surgery.
These preoperative issues have been shown to have lasting and intricate effects on
postoperative pain, fatigue, and depression. Therefore, it is imperative for clinical
doctors to promptly identify preoperative sleep disturbances and anxiety in order to
offer appropriate support to patients.
Colorectal cancer is the fifth leading cause of death in China, with nearly 40% of
patients experiencing insomnia before surgery, consistent with our previous studies. A
case-control study demonstrated a protective association between improved sleep quality
and relief of postoperative pain in colorectal cancers. Furthermore, individuals
undergoing laparoscopic colorectal surgery showed a higher likelihood of experiencing
visceral pain compared to somatic pain. Acute visceral pain has the potential to progress
into chronic visceral pain, resulting in behavioral manifestations such as anxiety, fear,
and depression, which may persist and exacerbate into enduring chronic pain, ultimately
impacting the individual's quality of life. Currently, studies have shown that disturbed
preoperative sleep has become a significant predictor of both acute and chronic
postoperative pain. Therefore, finding effective interventions to promote preoperative
sleep is a continuing consideration for clinicians.
Pharmacological intervention is the primary approach for preoperative sleep disturbances
or anxiety. Finding appropriate drug is a challenge that needs to be solved in the
clinical practice. There is currently a lack of evidence-based medical guidelines
regarding pharmacologic interventions for preoperative sleep disturbances and anxiety.
Research has indicated that zolpidem can enhance sleep quality in patients prior to
surgery, decrease the need for analgesics during the procedure, and alleviate
postoperative pain. Nevertheless, there is a demand for agents that possess both
short-term hypnotic and anxiolytic properties, whereas zolpidem solely exhibits hypnotic
effects. Midazolam, a short-acting benzodiazepine, is often used before anesthesia for
its short-term hypnotic and anxiolytic effects. Studies have found that midazolam oral
solution is safe and effective for short-term use in clinical pre-surgical settings.
There are no studies on using oral midazolam solution to improve sleep and reduce anxiety
in colorectal cancer patients before surgery. Our previous research found that a dose of
7.2mg can effectively induce sleep with minimal side effects in 50% patients before
surgery.
In summary, the present study intends to carry out a
prospective,randomized,double-blind,placebo-controlled clinical study to investigate the
hypothesis that preoperative oral midazolam solution could reduce acute postoperative
pain, promote early recovery, and reduce the risk of chronic pain in patients with poor
sleep or anxiety before colorectal cancer surgery. It is postulated that the potential
benefits of preoperative oral midazolam solution may be attributed to decreased stress
levels, and lowered inflammation markers.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
-
1. Signed of informed consent voluntarily; 2. Native Chinese speaker; 3. Age 18-60
years old, male or female; 4. BMI 18-30 kg/m2; 5. American Society of
Anesthesiologists (ASA) grade 1 or 2, New York Heart Association (NYHA)
gradeⅠor Ⅱ; 6. Non-emergency laparoscopic colorectal cancer resection; 7.
General anesthesia with tracheal intubation; 8. Sleep disturbance (the Insomnia
Severity Index,ISI≥15 ) or Anxiety (Generalized Anxiety Disorder
scale-7,GAD-7≥10 ) from admission to surgery.
Exclusion Criteria:
-
1. Contraindications for Midazolam Oral Solution (According to the Instruction for
Midazolam Oral Solution); 2. High risk of Obstructive Sleep Apnea Symptoms
(Total score of STOP-Bang scale ≥3 points); 3. Suspected dementia (Total score
of Mini-Mental State Examination (MMSE) according to years of education: 0
year≤19 points; 1~6 years≤22 points; above of 6 years≤26 points); 4. Severe
depressive symptom within two weeks (Total score of Patient Health
Questionnaire-9 (PHQ-9)≥15); 5. History of Neurological and Psychiatric
diseases (According to the electronic medical record system); 6. History of
Chronic Obstructive Pulmonary Disease (According to the electronic medical
record system); 7. History of Heart Failure (According to the electronic
medical record system); 8. Intestinal obstruction(The electronic medical record
system records those who currently have any type of intestinal obstruction); 9.
Liver and renal insufficiency; 10. Have taken opioids or drugs that act on the
central nervous system within one week; 11. Take CYP3A4 isoenzyme inhibitors or
inducers within one week (According to the Instruction for Midazolam Oral
Solution); 12. Consume any alcoholic beverage within 24 hours; 13. Substance
abusers (including alcohol, drugs or addictive substances); 14. Pregnant or
lactating women.
Gender:
All
Minimum age:
18 Years
Maximum age:
60 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
the Sixth Affiliated Hospital, Sun Yat-sen University
Address:
City:
Guangzhou
Zip:
510655
Country:
China
Start date:
July 2024
Completion date:
December 2025
Lead sponsor:
Agency:
Sixth Affiliated Hospital, Sun Yat-sen University
Agency class:
Other
Source:
Sixth Affiliated Hospital, Sun Yat-sen University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06407518