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Time to Eradication of Mycoplasma Genitalium and Chlamydia Trachomatis After Treatment Commenced

Primary Purpose

Urethritis, Cervicitis, Genital Mycoplasma Infection

Status
Unknown status
Phase
Phase 4
Locations
Sweden
Study Type
Interventional
Intervention
Azithromycin
Doxycycline
lymecycline
Sponsored by
Ostergotland County Council, Sweden
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urethritis focused on measuring Mycoplasma genitalium, Chlamydia trachomatis, Treatment, Antibiotic resistance

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Individuals attending the STD-clinic and being a sexual partner who has received an antibiotic treatment due to a non-specific urethritis/cervicitis or a confirmed Mycoplasma genitalium/Chlamydia trachomatis infection OR Having a confirmed infection described above or a symptomatic urethritis or cervicitis (non-gonorrhoic)

Exclusion Criteria:

  • Allergy against any of the drugs, woman being pregnant or breast feeding, Not speaking or understanding Swedish fluently. Other medication with possible interaction to given treatment

Sites / Locations

  • R&D dept of Local Health Care, Östergötland county councilRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Drug: Azithromycin 1g

Drug: Doxycycline/lymecycline 9/10days

Azithromycin 1.5 g

Arm Description

Azithromycin 1 g,single dose (per os)

Tetracycline either as Doxycycline or during June and July lymecycline (due to lower risk of photo-sensitivity) given for treatment in 9(10)days (per os).

Patients not randomized but receiving the first line treatment when a confirmed Mg infection

Outcomes

Primary Outcome Measures

Time from treatment starts to date of first negative test result is achieved up to 30 days.
Three arms. A randomisation (concealed envelopes) to either treatment with azithromycin 1g as a single dose or doxycycline for nine days (200 mg first day and 100 mg following nine (during summer time lymecycline 300mg twice daily for ten days). One un-randomized arm: Treatment with azithromycin 500 mg the first day and 250mg following four days or when indicated moxifloxacin 400 mg once daily for seven days.

Secondary Outcome Measures

Number of patients with emerging or existing macrolide resistance against Mycoplasma genitalium during or after treatment with azithromycin
Quantitive pcr of chlamydia and Mg is used. All Mg strains are tested for mutant genes.

Full Information

First Posted
July 27, 2012
Last Updated
December 12, 2014
Sponsor
Ostergotland County Council, Sweden
Collaborators
Statens Serum Institut
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1. Study Identification

Unique Protocol Identification Number
NCT01661985
Brief Title
Time to Eradication of Mycoplasma Genitalium and Chlamydia Trachomatis After Treatment Commenced
Official Title
Study of Time to Eradication of Mycoplasma Genitalium and Chlamydia Trachomatis After Antibiotic Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Unknown status
Study Start Date
February 2010 (undefined)
Primary Completion Date
August 2015 (Anticipated)
Study Completion Date
September 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ostergotland County Council, Sweden
Collaborators
Statens Serum Institut

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this on-going study is to study the number of days after antibiotic treatment has commenced (due to infection caused by the sexually transmitted bacteria Chlamydia trachomatis (CT) and Mycoplasma genitalium(Mg)) it takes to be cured i.e to get a negative test result. The specimens are analyzed on first-catch-urine (men) or patient's self-obtained vaginal sample with quantitive nucleic acid amplification test(NAAT). A secondary aim is to detect macrolide resistant Mg-strains and study whether there are any emerging macrolide resistant Mg-strains after treatment with azithromycin. A third aim is to study whether the participating subjects are adherent to the study protocol meaning 12 samples taken during a period of four weeks.
Detailed Description
Mycoplasma genitalium (Mg), detected in 1980, causes a urogenital infection through sexual transmission. In contrast to Chlamydia trachomatis antibiotic resistance is common against tetracyclines and is emerging against macrolides such as azithromycin. Both antibiotics are recommended as the first line treatment of chlamydia infection. Recent published data, however, indicate that 1g azithromycin stat may be only bacteriostatic when treating chlamydia. The consensus to date is that there should always be a test of cure in pregnant women having been treated for chlamydia and in all individuals treated for Mg. There are no studies published, to our knowledge, where the time to eradication after antibiotic treatment commenced in Mg infection has been evaluated. The first line treatment of a confirmed Mg infection is azithromycin 1.5 g given during a period of 5 days. If macrolide resistance is plausible or confirmed moxifloxacin 400mg for 7 to 10 days is recommended. Individuals with symptomatic urethritis or cervicitis and/or being sexual partners to individuals being treated for a suspect or confirmed Mg or CT infection were eligible. The study subjects were patients attending either of the STD-clinics in Norrköping or Västervik, Sweden. All samples were sent to Statens Serum Institut(SSI), Mycoplasma department (Jorgen Skov Jensen) for analysis. Patients accepting enrolment with a confirmed or highly suspected Mg were receiving azithromycin 500 mg the first day and 250mg the following four days. Patients where macrolide resistant Mg-strain infection was highly suspected received moxifloxacin 400 mg once daily for seven days. Those subjects intended to treatment but with a lower degree of suspicion of Mg infection were randomized to either a treatment with doxycycline 200 mg the first day and 100 mg once daily the following nine days (the custom and recommendation in Sweden for treatment of chlamydia and non-specific urethritis or cervicitis) OR a treatment with azithromycin 1g as a single dose. All participants were given test kits for 12 samples, which were to be sampled three times weekly (every second day) during four weeks starting the day after the first day of treatment. They were instructed not to have any sexual intercourse during the first week and with condom afterwards during the study period. The samples were to be sent once weekly (three samples)to SSI.The date of sampling was to be noted on the label of the tube and the attaching paper to SSI, where also any symptoms were to be noted. The results of the tests were sent to the STD-clinic who informed the patient. The study started in February 2010 and inclusion of patients have ended for those subjects with a verified M genitalium infection (February 2014), whereas patients with a verified or suspected chlamydia infection still are enrolled and randomised to azithromycin 1 g or doxycycline. A manuscript will soon be submitted concerning those subjects being treated for a M genitalium infection. To date 190 patients have been enrolled and also fulfilled the study protocol with sampling of specimens.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urethritis, Cervicitis, Genital Mycoplasma Infection, Chlamydia Trachomatis
Keywords
Mycoplasma genitalium, Chlamydia trachomatis, Treatment, Antibiotic resistance

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Drug: Azithromycin 1g
Arm Type
Active Comparator
Arm Description
Azithromycin 1 g,single dose (per os)
Arm Title
Drug: Doxycycline/lymecycline 9/10days
Arm Type
Active Comparator
Arm Description
Tetracycline either as Doxycycline or during June and July lymecycline (due to lower risk of photo-sensitivity) given for treatment in 9(10)days (per os).
Arm Title
Azithromycin 1.5 g
Arm Type
Active Comparator
Arm Description
Patients not randomized but receiving the first line treatment when a confirmed Mg infection
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Other Intervention Name(s)
Zitromax, Azitromax
Intervention Description
In the randomized arm giver orally 1 g as a single dose. In the non-randomized arm given for 5 days 250mg 2x1 first day and 1x1 following four days.
Intervention Type
Drug
Intervention Name(s)
Doxycycline
Other Intervention Name(s)
Doxyferm
Intervention Description
Doxycycline tablets 100 mg 2x1 the first day and 100 mg daily for following eight days (following the Swedish tradition and experience since the 1970s of treating chlamydia)
Intervention Type
Drug
Intervention Name(s)
lymecycline
Other Intervention Name(s)
Tetralysal 300mg
Intervention Description
Lymecycline 300 mg twice daily for 10 days (Summertime due to less risk of phototoxic reactions)
Primary Outcome Measure Information:
Title
Time from treatment starts to date of first negative test result is achieved up to 30 days.
Description
Three arms. A randomisation (concealed envelopes) to either treatment with azithromycin 1g as a single dose or doxycycline for nine days (200 mg first day and 100 mg following nine (during summer time lymecycline 300mg twice daily for ten days). One un-randomized arm: Treatment with azithromycin 500 mg the first day and 250mg following four days or when indicated moxifloxacin 400 mg once daily for seven days.
Time Frame
From first day of treatment to date of first negative test up to 30 days per subject
Secondary Outcome Measure Information:
Title
Number of patients with emerging or existing macrolide resistance against Mycoplasma genitalium during or after treatment with azithromycin
Description
Quantitive pcr of chlamydia and Mg is used. All Mg strains are tested for mutant genes.
Time Frame
One month after treatment has started
Other Pre-specified Outcome Measures:
Title
Number or rate of patients adherent regarding sampling according to the protocol
Description
To describe whether the subjects are adherent to the study protocol according to doing the sampling and sending the samples correctly.
Time Frame
One month after starting sampling

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Individuals attending the STD-clinic and being a sexual partner who has received an antibiotic treatment due to a non-specific urethritis/cervicitis or a confirmed Mycoplasma genitalium/Chlamydia trachomatis infection OR Having a confirmed infection described above or a symptomatic urethritis or cervicitis (non-gonorrhoic) Exclusion Criteria: Allergy against any of the drugs, woman being pregnant or breast feeding, Not speaking or understanding Swedish fluently. Other medication with possible interaction to given treatment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lars Falk, MD PhD
Phone
+46 10 103 8507
Email
lars.falk@lio.se
First Name & Middle Initial & Last Name or Official Title & Degree
Jorgen S Jensen, MD DrMedSci
Email
jsj@ssi.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lars Falk, MD PhD
Organizational Affiliation
Dept of Derm&Venereology Linköping University hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
R&D dept of Local Health Care, Östergötland county council
City
Linköping
ZIP/Postal Code
SE-58185
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lars Falk, MD PhD
Email
lars.falk@lio.se

12. IPD Sharing Statement

Citations:
PubMed Identifier
26283670
Citation
Falk L, Enger M, Jensen JS. Time to eradication of Mycoplasma genitalium after antibiotic treatment in men and women. J Antimicrob Chemother. 2015 Nov;70(11):3134-40. doi: 10.1093/jac/dkv246. Epub 2015 Aug 17.
Results Reference
derived

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Time to Eradication of Mycoplasma Genitalium and Chlamydia Trachomatis After Treatment Commenced

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