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Effect of SmtO2 Guided Care on PONV (iMODIPONV)

Effect of Muscular Tissue Oxygen Saturation-Guided Management During Laparoscopic Hysterectomy on Postoperative Nausea and Vomiting: A Randomized Controlled Trial (iMODIPONV)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03641625
Acronym
iMODIPONV
Enrollment
800
Registered
2018-08-22
Start date
2018-09-15
Completion date
2019-07-31
Last updated
2019-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Pressure Management, Cardiac Output Management, Hysterectomy, Postoperative Nausea and Vomiting, Tissue Oxygenation

Keywords

Postoperative Nausea and Vomiting, Laparoscopic Hysterectomy, Muscular Tissue Oxygen Saturation, Hemodynamic Management

Brief summary

This randomized controlled trial is to investigate if SmtO2-guided management on top of the usual care, compared with the usual care only, during laparoscopic hysterectomy significantly reduces the incidence of PONV.

Detailed description

Postoperative nausea and vomiting (PONV) remains prevalent despite the institution of various prophylactic measures. The incidence of PONV in female patients undergoing laparoscopic gynecological surgery is up to 50% with and 70% without the administration of antiemetics, respectively. The consequences of PONV range from patient discomforts, postoperative complications, prolonged hospitalization, to increased health care costs. Among the multiple risk factors, suboptimal gastrointestinal (GI) perfusion or oxygenation may be responsible for some cases of PONV; however, this speculation remains to be confirmed.5 Optimal tissue oxygenation, the balance between tissue oxygen consumption and supply, is essential for the integrity of any tissue bed that is metabolically active. However, GI oxygenation cannot be directly and continuously monitored in patients at this time. Whether there is an organ which can be used as a surrogate of the GI system, meaning that the tissue oxygenation of this surrogate organ not only can be monitored and that it also correlates with that of the GI system, is an intriguing question. Currently, tissue oxygenation can be measured using near-infrared spectroscopy (NIRS) in patients. The recent advancements of this technology enable the accurate monitoring of the oxygenation within many tissue beds depending on the location of the oximetry probe. The recent cohort study demonstrated that there is a close relationship between muscular tissue oxygen saturation (SmtO2) and PONV in patients undergoing robotic laparoscopic hysterectomy (manuscript accepted and in production). Multiple thresholds based on threshold, AUC, and multivariable analyses are able to differentiate the risk of PONV. The following SmtO2 thresholds were found to correlate with a reduced risk of PONV: 20% above baseline; while the following thresholds correlate with an increased risk of PONV: 5% below baseline, 15% below baseline, and 20% below baseline, \< 70%, \< 65%, and \< 60%. Taken together, our study suggests the potential therapeutic targets for PONV prophylaxis may be to maintain SmtO2 \> 70% and above baseline. In this study, the investigators aim to investigate if intraoperative care guided by SmtO2 monitoring reduces the incidence of PONV after laparoscopic hysterectomy.

Interventions

DEVICEMuscular tissue oxygen saturation guided care

Muscular tissue oxygen saturation monitored at flank and arm will be maintained \> 70% (absolute measurement) and \> baseline throughout the entire procedure.

Sponsors

The Second Hospital of Hebei Medical University
CollaboratorOTHER
Peking University First Hospital
CollaboratorOTHER
Peking University Third Hospital
CollaboratorOTHER
Shandong Provincial Hospital
CollaboratorOTHER_GOV
The First Affiliated Hospital of Zhengzhou University
CollaboratorOTHER
Beijing Obstetrics and Gynecology Hospital
CollaboratorOTHER
Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Both patients and outcomes assessor are blinded to group assignment.

Intervention model description

International, multi-center, pragmatic, randomized controlled (1:1 ratio) trial

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Age 18-65 years 2. Non-smoker 3. ASA I-III 4. Elective laparoscopic procedure involving hysterectomy

Exclusion criteria

1. Refuse to participate 2. Emergent surgery 3. Bowel resection planned 4. Vaginal or abdominal (open) hysterectomy 5. Chemotherapy or radiotherapy before surgery 6. Significant neuro, cognitive, or psychologic disease: stroke with neurologic deficit, dementia, schizophrenia, or any condition that makes meaningful postoperative follow-ups impossible 7. Significant cardiovascular disease: low-output cardiac failure defined as a preoperative left ventricular ejection fraction \< 30%, active coronary artery disease, symptomatic valvular disease, symptomatic arrhythmia with or without pacemaker and/or AICD placement 8. Significant pulmonary disease: COPD requiring home oxygen therapy, severe asthma requiring steroid treatment, other pulmonary conditions requiring home oxygen therapy 9. Severe hepatic dysfunction being evaluated for liver transplantation or with a Child-Pugh Class C classification 10. Severe renal dysfunction requiring renal replacement therapy 11. Muscular pathologies such as dystrophy, atrophy, and weakness 12. Skin conditions incompatible with the adhesive oximetry probe (e.g., delicate or tattooed skin) 13. Current or previous smoker 14. ASA Physical Score ≥ IV

Design outcomes

Primary

MeasureTime frameDescription
Incidence of PONV within 24 hours after surgeryup to 24 hoursNausea: Nausea is defined as a subjective unpleasant sensation associated with the urge to vomit. Retching: Retching is defined as the labored, spastic, and rhythmic contraction of chest and abdominal muscles without expulsion of gastric contents. Vomiting: Vomiting is defined as the forceful expulsion of any gastric contents from the mouth. PONV: PONV refers to the occurrence of nausea, retching, and/or vomiting.

Secondary

MeasureTime frameDescription
Severity of postoperative painup to 24 hoursPostoperative pain intensity at rest and with movement expressed using NRS 0-10 (0 = no pain; 10 = worst pain) at 2, 6, and 24 h depending on the time to discharge
Time of GI recoveryup to 48 hoursTime to GI recovery (time to first flatus, bowel motion, and/or time to tolerate oral diet, in hours)
Overall quality of recovery based on QoR-15 questionnaireup to 24 hoursPostoperative quality of recovery (using the QoR-15 questionnaire) QoR-15 Questions PART A How have you been feeling in the last 24 hours? (0 to 10, where 0 = none of the time \[poor\] and 10 = all of the time \[excellent\] Q.1 Able to breathe easily Q.2 Been able to enjoy food Q.3 Feeling rested Q.4 Have had a good sleep Q.5 Able to look after personal toilet and hygiene unaided Q.6 Able to communicate with family or friends Q.7 Getting support from hospital doctors and nurses Q.8 Able to return to work or usual home activities Q.9 Feeling comfortable and in control Q.10 Having a feeling of general well-being PART B Have you had any of the following in the last 24 hours? (10 to 0, where 10 = none of the time \[excellent\] and 0 = all of the time \[poor\]) Q.11 Moderate pain Q.12 Severe pain Q.13 Nausea or vomiting Q.14 Feeling worried or anxious Q.15 Feeling sad or depressed
Time to mobilizationup to 48 hoursTime to mobilization (time to first out-of-bed mobilization, in hours)
Score of sleep qualityup to 48 hoursPostoperative sleep quality (using NRS 0-10 (0 = no concern at all; 10 = worst ever) for the first night or the second night if the case is finished after 6pm)
Incidence of early PONVup to 6 hoursThe incidence of PONV during postoperative 0-6 hours. The diagnostic criteria for early PONV are the same as above (outcome 1).
Non-GI-related composite complicationsup to 30 daysBoth in-hospital and 30-day non-GI-related composite complications (Complication was defined as any deviation from the normal postoperative course or organ dysfunction.\[23-25\] Organ-specific complications include myocardial infarction, congestive heart failure, cardiac arrest, atrial fibrillation or other types of arrhythmia, pulmonary embolus, pneumonia treated with antibiotics, respiratory failure requiring intubation, respiratory insufficiency requiring physiotherapy or oxygen therapy, stroke, transient ischemic attack, postoperative delirium or cognitive decline, renal insufficiency requiring dialysis, acute kidney injury, urinary tract infection requiring antibiotics, hepatic insufficiency, gut hypoperfusion, ileus, disseminated intravascular coagulation, and sepsis. Surgery-related complications refer to surgical site bleeding, infection, anastomotic leakage, stenosis, ischemia, or tissue necrosis.)
Length of hospital stayup to 30 daysLength of hospital stay, in days
Rate of ICU admissionUp to 30 daysThe percentage of patients admitted to ICU after surgery
30-day mortality30 days30-day mortality
In-hospital GI complicationsup to 30 daysIn-hospital GI-related composite complication (composite of ileus, obstruction, perforation, and bleeding)

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026