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CompletedNCT02005263Updated Nov 8, 2017

Hysteroscopic Assessment of Fallopian Tubal Patency

An interventional study of Salpingography in Infertility and Menorrhagia, sponsored by University of Mississippi Medical Center. Completed at 1 site in United States. Open to female participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2017-11-08.

Sponsored by University of Mississippi Medical Center · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
621
Allocation
Not applicable
Ages
18 Years to 50 Years
Sex
Female
01

Study summary

Disease of the fallopian tubes is one of the most common reasons for infertility. The most common test, a hysterosalpingogram, tends to be painful,inconvenient, and frequently misses concurrent uterine disease. We propose using a less painful technique (through modified office hysteroscopy) for tubal assessment that can be performed in the office rather than hospital radiology and that uses gold standard technology for identifying coexisting uterine conditions.

02

Conditions studied

  • Infertility
  • Menorrhagia

Keywords

  • Hysteroscopy
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In context

Infertility

2,506 studies on the registry are indexed under Infertility; 407 are open to participants now.

This study's enrollment of 621 is above the median of 120 across 1,698 interventional studies indexed under Infertility.

Browse Infertility studies →

Lead sponsor

University of Mississippi Medical Center is the lead sponsor of 125 studies on the registry; 19 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 4 (57%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  1. 18 - 50 years old
  2. Able to give consent
  3. Must have a uterus
  4. Must have documented negative testing for gonorrhea and chlamydia within the past year or previously negative when tested with a current partner in a monogamous relationship
  5. Negative test prior to procedure

Exclusion criteria

Exclusion Criteria:

  1. Pregnancy
  2. Active lower and upper genital tract infection
  3. Patients with allergies to hysterosalpingogram contrast will not be exposed to a contrast material to which they are allergic
  4. Premenarchal or postmenopausal
  5. Unable to read English at a 6th grade level or above
  6. History of endometrial Ablation
  7. Asherman's syndrome > Stage 1
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
621 participants (actual)

Study arms

  • Experimental
    Salpingography

    Infusion of air bubbles through Fallopian tubes with hysteroscopic visualization; typically 1-2 mL is infused. This is less than that typically used in the established technique of sonosalpingography.

    Procedure: Salpingography

Interventions

  • ProcedureSalpingography

    Infusion of typically 1-2 mL of air bubbles in to the uterine cavity to assess whether they disappear through the ostia in to the Fallopian tubes.

    Also known as: Parryscope technique

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What researchers measure

Primary outcomes

  1. Hysteroscopic assessment of tubal patency

    Patients undergoing the procedure will be informed based on the findings as to whether or not it is believed that their Fallopian tubes are patent

    Time frame: 2 years

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Study locations

1 site
  • University of Mississippi Medical Center
    Jackson, Mississippi 39216, United States
08

References and documents

Publications

  • Parry JP, Riche D, Rushing J, Linton B, Butler V, Lindheim SR. Performing the Parryscope technique gently for office tubal patency assessment. Fertil Steril. 2017 Oct;108(4):718. doi: 10.1016/j.fertnstert.2017.07.1159. Epub 2017 Aug 31. PubMed 28843382 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 8, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02005263
Lead sponsor
University of Mississippi Medical Center
Responsible party
John Preston Parry, MD, MPH (Assistant Professor, University of Mississippi Medical Center) — Principal investigator
First posted
Dec 9, 2013
Start date
Dec 2013
Primary completion
Oct 16, 2017
Completion
Nov 6, 2017
Last update
Nov 8, 2017

Study contacts

John P. Parry, MD
principal investigator · University of Mississippi Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2017. You cannot join it, but the record below documents what was studied.

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