3 mL Inhaled Methoxyflurane for Intrauterine Device (IUD) Insertion
NCT07295054 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 110
Last updated 2026-05-11
Summary
Intrauterine device (IUD) insertion is a common contraceptive procedure often associated with moderate to severe pain, particularly among nulliparous individuals. Current pain management strategies, such as over-the-counter analgesics, are frequently inadequate. Methoxyflurane, a short-acting, self-administered inhaled analgesic, has been shown to provide rapid and effective pain relief in acute and procedural settings. This study aims to evaluate whether 3 mL of inhaled Methoxyflurane (via Penthrox inhaler) improves patient satisfaction by reducing pain and anxiety during IUD insertion.
Conditions
- IUD
Interventions
- DRUG
-
Methoxyflurane
3 mL of Methoxyflurane via a handheld inhaler
- DRUG
-
Saline
3 mL of Normal Saline via an identical placebo handheld inhaler
Sponsors & Collaborators
-
Women's College Hospital
lead OTHER
Principal Investigators
-
Lauren Scott, NP · Women's College Hospital
-
Karim Ladha, MD · Women's College Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-04-27
- Primary Completion
- 2026-12-31
- Completion
- 2027-02-28
Countries
- Canada
Study Locations
More Related Trials
-
PK of Depo SubQ Injected in the Upper Arm
NCT01143207 ·Status: COMPLETED ·Phase: NA
-
Mirena Intrauterine System Timing of Insertion: A Randomized Controlled Trial
NCT01272960 ·Status: COMPLETED ·Phase: NA
-
Prospective, Non-interventional, Multi-center Safety Study of Mirena for Heavy Menstrual Bleeding and Dysmenorrhea
NCT02475356 ·Status: COMPLETED
-
A Study to Assess the Safety of a New Inserter Device for Paragard® (Intrauterine Copper Contraceptive)
NCT05309694 ·Status: COMPLETED ·Phase: PHASE4
-
Study of a Levonorgestrel 52 mg Intrauterine System for the Treatment of Heavy Menstrual Bleeding
NCT03642210 ·Status: COMPLETED ·Phase: PHASE3
-
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
NCT02509767 ·Status: COMPLETED ·Phase: PHASE4
-
Quick Start Insertion of Mirena and ParaGard
NCT01730911 ·Status: COMPLETED ·Phase: NA
-
Innovative Model of Patient-Centered ConTraception
NCT02364037 ·Status: COMPLETED ·Phase: NA
-
Study of the Copper IUD or Oral Levonorgestrel and the Levonorgestrel IUD for Women Seeking Emergency Contraception
NCT01963962 ·Status: COMPLETED
-
An Explorative Trial to Explore the Safety, Acceptability and Vaginal Bleeding Pattern of Three Etonogestrel-releasing Medicated Intrauterine Systems (Study P06060)
NCT00967746 ·Status: COMPLETED ·Phase: PHASE2
-
Bleeding Pattern and User Satisfaction During Second Consecutive MIRENA® in Contraception and Treatment of Menorrhagia
NCT00393198 ·Status: COMPLETED ·Phase: PHASE4
-
A proof-of Concept, Randomized 3-month Study to Evaluate the Effects of Three Contraceptive Intrauterine Systems Delivering Copper and a Daily Dose of 5, 20 or 40 μg of Ulipristal Acetate (UPA)
NCT03230539 ·Status: UNKNOWN ·Phase: PHASE1
-
Study on Medical Records of Women Using an Intrauterine Device (IUD) to Analyze the Risks That the IUD Will be Expelled or Perforates the Womb in Relation to Breastfeeding, the Point in Time When the IUD Was Inserted After Childbirth and in Relation to Different Types of IUDs
NCT03754556 ·Status: COMPLETED
-
A Study to Investigate the Contraceptive Efficacy and Safety of a Subdermal Etonogestrel Implant (Implanon®)(P06473)(COMPLETED)
NCT00725413 ·Status: COMPLETED ·Phase: PHASE4
-
Oral Levonorgestrel Plus Meloxicam, IG-002 Delays Ovulation in Normal Menstruating Women by Seven Days
NCT05695352 ·Status: RECRUITING ·Phase: PHASE2
-
Safety and Efficacy of CDB-2914 for Emergency Contraception
NCT00411684 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Evaluate the Safety and Efficacy of Two Contraceptive Vaginal Rings Delivering a Daily Dose of 1500 or 2500 μg of CDB-2914
NCT00791297 ·Status: COMPLETED ·Phase: PHASE2
-
Levonorgestrel 52 mg IUD for Emergency Contraception and Same-Day Start
NCT05444582 ·Status: RECRUITING ·Phase: PHASE4
-
A Pharmacokinetics, Pharmacodynamics, and Safety Study of an Oral Contraceptive Containing Norethindrone and Ethinyl Estradiol When Co-administered With GSK1322322 in Healthy Adult Women
NCT01953809 ·Status: WITHDRAWN ·Phase: PHASE1
-
HR-QoL and Sexuality in Mirena Inserted Contraception Users
NCT00498784 ·Status: COMPLETED ·Phase: PHASE4
-
Self Administration of Subcutaneous Depot Medroxyprogesterone Acetate
NCT00770887 ·Status: COMPLETED
-
Immediate Postplacental IUD Insertion
NCT02169869 ·Status: TERMINATED ·Phase: NA
-
Modulation of Mucosal and Systemic Immunity by Hormonal Contraceptives
NCT01750476 ·Status: TERMINATED
-
Safety of the Etonogestrel-releasing Implant During the Puerperium of Healthy Women
NCT00828542 ·Status: COMPLETED ·Phase: NA
-
Maintaining Intrauterine Devices (IUDs) in Teens (MINT): A Randomization Trial
NCT00653159 ·Status: COMPLETED ·Phase: PHASE4