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Fast-Release Orodispersible Tramadol Tablet (Tradonal Odis®) as Analgesia for Hysterosalpingography

Fast-Release Orodispersible Tramadol Tablet (Tradonal Odis®) as Analgesia for Hysterosalpingography : a Randomized, Controlled, Double Blinded Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00893412
Enrollment
128
Registered
2009-05-06
Start date
2008-11-30
Completion date
2009-04-30
Last updated
2009-05-06

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

Conditions

Infertility, Pain

Keywords

HSG, analgesia, tramadol, metal cannula, balloon catheter

Brief summary

This study evaluates the analgetic effects of the fast-release orodispersible tramadol tablet. Tramadol acts through a weak affinity for μ receptors and secondly by inhibiting noradrenaline and serotonin neuronal reuptake. It has been used since the 1970s by over 50 million people for the treatment of acute and chronic pain. The orodispersible Tramadol tablet is a new galenic form and is available on the Belgian market for the last three years. Pregastric absorption leads to a quicker onset of action. So far, evidence shows that pain during and immediately after the Hysterosalpingography (HSG) procedure is only significantly reduced by IV opioid analgesia. This study evaluates the analgetic potential of an orodispersible opioid tablet. This tablet disintegrates rapidly (in around 20-30 seconds) and may be taken without water. Its abuse potential is very low and its respiratory depressant effect is negligible.

Detailed description

Four arm prospective randomized double blinded trial Patients that need a HSG as part of their diagnostic work-up and are eligible for randomization are counseled about possible participation. After signing the informed consent patients will be randomized in one of the following four groups: Group 1: Fast-release Orodispersible Tramadol Tablet + metal cannula Group 2: Placebo + metal cannula Group 3: Fast-release Orodispersible Tramadol Tablet + balloon catheter Group 4: Placebo + balloon catheter Tablets are administered 30 min before the procedure Primary Endpoint: * VAS at the six different assessment points Secondary Endpoint * adverse effects and complications such as: nausea, vomiting, constipation, drowsiness, respiratory depression, hypotension, allergic reaction and infection

Interventions

DRUGFast-release Orodispersible Tramadol Tablet (Tradonal odis®)

1 tablet of 50 mg Fast-release Orodispersible Tramadol Tablet (Tradonal odis®)

PROCEDUREHysterosalpingography (HSG)

One HSG using a metal canula or balloon catheter, 30 minutes after tablet

DRUGPlacebo

Sponsors

Universitair Ziekenhuis Brussel
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* \> 18 and \< 45 years * Written informed consent

Exclusion criteria

* Contra-indication to tramadol, morphine or to other opioids * Concomitant use of MAO inhibitors or use less than 2 weeks prior to procedure * Use of any other CNS-acting drug * Contra-indication to radio-contrast medium (allergy) * Patient already taking analgetics * History of cervical stenosis * Presence of pelvic inflammatory disease or any other condition causing pelvic pain * Clinical and/or laboratory evidence of any major disease * Pregnant or lactating

Design outcomes

Primary

MeasureTime frame
VAS at the six different assessment points24 hours

Secondary

MeasureTime frame
Adverse effects and complications24 hours

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026