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Completed

NCT Number: NCT03052816

Ice T Postoperative Multimodal Pain Regimen in FPMRS Surgery

The purpose of this randomized controlled trial is to determine whether, "ICE-T," a novel multimodal postoperative pain regimen composed of around the clock ice packs, toradol, and tylenol, has improved pain control intake compared to the standard postoperative pain regimen in patients undergoing vaginal pelvic floor reconstructive surgery.

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Key information

Age range

18 year–80 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

University Hospitals Case Medical Center

Cleveland, Ohio, 44106, United States

About this study

Pelvic floor disorders involve a myriad of complicated, interwoven clinical conditions that involve pelvic organ prolapse, urinary incontinence, fecal incontinence, and other pathology involving the genital and lower urinary tract. It is estimated that pelvic floor disorders affect up to 25% of all adult women in the United States with increasing prevalence with age. By the age of sixty, 1 in 9 women will undergo surgical intervention for pelvic organ prolapse and/or incontinence, increasing to 1 in 5 by the age of 80. As the population in the United States ages, the demand for healthcare for pelvic floor disorders is estimated to increase up to 40% in the next 30 years.

Despite the prevalence of surgery performed for pelvic floor disorders, there is a paucity of data on postoperative pain control that is dedicated to female pelvic reconstructive surgery. In a recent review, there was only one study that evaluated postoperative pain control after vaginal reconstructive surgery, and the mainstay of therapy was opioid driven. Generally, postoperative pain control in gynecologic surgery has been opioid driven, frequently involving multiple narcotics for analgesia, resulting opioid related complications, including nausea, vomiting, constipation, urinary retention, and central nervous system side effects In an effort to combat opioid use in gynecologic and female pelvic reconstructive surgery, multimodal therapy has been gaining momentum with goals of improved pain control and decreased opioid requirements. Ice packs, toradol, and acetaminophen have been used in various trials to decrease postoperative opioid requirements in various surgeries.

Ice packs have been shown to be effective in the treatment of postoperative pain after abdominal midline incisions. A Cochrane Review of patients subject to post vaginal delivery perineal cooling included 10 randomized controlled trials with1825 patients with some evidence that local cooling in the form of ice packs, cold gel packs, cold/ice backs may be effective in pain relief.

Toradol has been extensively studied in a multitude of surgeries including spinal, obstetric, orthopedic, urologic, and gynecologic. It has been administered preemptively, intraoperatively, and postoperatively for pain control with evidence that toradol decreases postoperative subjective pain scores and decreased narcotic use.

Acetaminophen is mainstay for postoperative pain control as part of multimodal pain regimens to complement other, opioid sparing medications in a multitude of surgeries including abdominal hysterectomy.

Therefore, the purpose of this randomized controlled study is to determine whether, "ICE-T" a novel multimodal postoperative pain regimen composed of around the clock ice packs, toradol, and tylenol, has improved pain control and decrease opioid intake compared to the standard postoperative pain regimen in patients undergoing vaginal pelvic floor reconstructive surgery.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The inclusion criteria are the following:
  • Consenting, English speaking women between ages 18 and 80 who will undergo same day vaginal female pelvic reconstructive surgery at MetroHealth Medical Center
  • Ability to read VAS Scores
  • Specific vaginal procedures include, but are not limited to:
  • Periurethral bulking
  • Perineoplasty
  • Complete vaginectomy
  • Le Forte colpocleisis
  • Anterior repair
  • Posterior repair
  • Enterocele repair
  • Anterior and posterior repair
  • Anterior, posterior and enterocele repair
  • Transvaginal mesh use
  • Sacrospinous ligament fixation
  • Uterosacral ligament suspension
  • Vaginal paravaginal defect repair
  • Midurethral Sling
  • Sphincteroplasty
  • Vaginal hysterectomy, for uterus 250 g or less
  • Vaginal hysterectomy, for uterus 250 g or less; with removal of tube(s), and/or ovary(s)
  • Vaginal hysterectomy, for uterus 250 g or less; with removal of tube(s), and/or ovary(s), with repair of enterocele
  • Vaginal hysterectomy, for uterus 250 g or less; with repair of enterocele
  • Vaginal hysterectomy, for uterus greater than 250 g
  • Vaginal hysterectomy, for uterus greater than 250 g; with removal of tube(s) and/or ovary(s)
  • Vaginal hysterectomy, for uterus greater than 250 g; with removal of tube(s) and/or ovary(s), with repair of enterocele
  • Vaginal hysterectomy, for uterus greater than 250 g; with repair of enterocele

Exclusion criteria

  • The exclusion criteria are the following:
  • History of chronic pelvic pain
  • Abdominal surgery
  • Laparoscopic surgery
  • History of psychiatric disease
  • Currently taking analgesic medications
  • Currently taking sedatives
  • Liver disease
  • Renal disease with CrCl < 60cc/min.
  • History of burns from application of ice.
  • Women who did not consent for the study.
  • Intraoperative concern for increased blood loss
  • Unable to speak English
  • Unable to understand VAS Scores
  • Undergoing concomitant abdominal or laparoscopic procedures.
  • Allergy to motrin, toradol, Percocet, Tylenol
  • Active or history of peptic ulcer disease
  • History of GI bleeding or perforation
  • Hemorrhagic diathesis
  • Severe uncontrolled heart failure
  • Inflammatory bowel disease

Treatment and study plan

Ice T

Drug

Ice/Tylenol/Toradol with dilaudid for breakthrough

Motrin/Percocet/Dilaudid for breakthrough

Drug

Standard regimen

Primary outcomes

  1. Visual Analog Scores (VAS)

    Time frame: Visual Analog Scores (VAS) Score in the morning of post op day 1 at 7am.

    Visual Analog Scores (VAS) Scores in the morning of post op day 1. The VAS is a 100mm scale with a score of no pain on the left of the scale, indicating a score of 0, and a score of worst pain on the right, indicating a score of 10. Patient is instructed to score the scale where they feel is appropriate. Each demarcation in between marks is 10mm and after the patient marks their score it is measured using mm from 0mm-100mm. A score of 0 is 0mm and a score of 10 is 100mm.

Secondary outcomes

  1. VAS Scores at 4 Hours Post Surgery

    Time frame: VAS Scores at 4 hours post surgery

    VAS Scores at 4 hours post surgery. The VAS is a 100mm scale with a score of no pain on the left of the scale, indicating a score of 0, and a score of worst pain on the right, indicating a score of 10. Patient is instructed to score the scale where they feel is appropriate. Each demarcation in between marks is 10mm and after the patient marks their score it is measured using mm from 0mm-100mm. A score of 0 is 0mm and a score of 10 is 100mm.

  2. VAS Scores 96 Hours After Surgery

    Time frame: VAS Scores 96 hours after surgery

    VAS Scores 96 hours after surgery. The VAS is a 100mm scale with a score of no pain on the left of the scale, indicating a score of 0, and a score of worst pain on the right, indicating a score of 10. Patient is instructed to score the scale where they feel is appropriate. Each demarcation in between marks is 10mm and after the patient marks their score it is measured using mm from 0mm-100mm. A score of 0 is 0mm and a score of 10 is 100mm.

  3. Quality of Recovery Scores on Post op Day 1

    Time frame: Quality of Recovery scores on post op day 1

    Quality of Recovery scores on post op day 1. The QoR-40 is a 40-item quality of recovery score measuring 5 dimensions: physical comfort (12 items), emotional state (9 items), physical independence (5 items), psychological support (7 items), and pain (7 items). Each item is rated on a 5-point Likert scale. The QoR-40 has a possible score of 40 (extremely poor quality of recovery) to 200 (excellent quality of recovery). It was specifically designed to measure a patient's health status after surgery and anesthesia, and it has been proposed as a measure of outcome in clinical trials.

  4. Satisfaction Scores in the Morning After Surgery (7AM)

    Time frame: Satisfaction scores in the morning after surgery (7AM)

    Satisfaction scores in the morning after surgery (7AM). The satisfaction score is a numerical score from 0-10 with a score of 0 indicating very dissatisfied on the left of the scale and 10 indicating very satisfied on the right of the scale.

  5. Satisfaction Scores 96 Hours After Surgery

    Time frame: Satisfaction scores 96 hours after surgery

    Satisfaction scores 96 hours after surgery. The satisfaction score is a numerical score from 0-10 with a score of 0 indicating very dissatisfied on the left of the scale and 10 indicating very satisfied on the right of the scale.

  6. Length of Stay

    Time frame: Time from end of surgery to discharge home from hospital, assessed up to 1 week.

    Length of time from the end of surgery to discharge home from the hospital, assessed up to 1 week.

  7. Total Dose of Opioids Administered During Hospitalization

    Time frame: Total dose of opioids administered during hospitalization in morphine equivalents from the end of surgery to discharge up to 1 week

    Total dose of opioids administered during hospitalization in morphine equivalents upon hospital discharge.

  8. Postoperative Nausea and Vomiting at 7AM After Surgery

    Time frame: Postoperative nausea and vomiting from the time to end of surgery until 7AM after surgery

    Number of patients with postoperative nausea and vomiting at 7AM after surgery

  9. Number of Participants With Urinary Retention.

    Time frame: Number of participants with urinary retention (discharge home with foley) measured on day patient is discharged home/study completion up to 1 week.

    Number of participants with urinary retention (discharge home with foley)

Sponsors and collaborators

Lead sponsor

University Hospitals Cleveland Medical Center

Other

Registry information

Official study title

ICE-T Postoperative Multimodal Pain Regimen Compared to the Standard Regimen in Same Day Vaginal Pelvic Reconstructive Surgery: a Randomized Controlled Trial

Acronym: ICET

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Feb 14, 2017
Registry last updated
May 19, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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