Trial of the Use of Doxycycline After Rotator Cuff Repair
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT02388477 |
Recruitment Status :
Withdrawn
(Research idea tabled at this point.)
First Posted : March 17, 2015
Last Update Posted : May 9, 2016
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Rotator Cuff Injury | Drug: Doxycycline Drug: sugar pill | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 0 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Single (Participant) |
Primary Purpose: | Treatment |
Official Title: | Randomized Controlled Trial of the Use of Doxycycline After Rotator Cuff Repair |
Estimated Primary Completion Date : | May 2016 |

Arm | Intervention/treatment |
---|---|
Active Comparator: Doxycycline
oral doxycycline, 2 weeks, twice a day,
|
Drug: Doxycycline
antibiotic used to treat infection
Other Names:
|
Placebo Comparator: sugar pill
sugar pill, same size, shape, and color as comparator, twice a day for 2 weeks.
|
Drug: sugar pill
placebo with no pharmacologic effect |
- rotator cuff ultrasound of post-operative shoulder [ Time Frame: one year ]An ultrasound of the post-operative rotator cuff to assess level of healing or defect present.
- American Shoulder and Elbow Surgeons score [ Time Frame: 6 weeks, 3mos, 6mos, 1yr and 2 yr. ]The survey is a standardized assessment of shoulder pain and function from the patient's perspective.

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- repair of rotator cuff
- age 18 and above
- able to swallow capsules
Exclusion Criteria:
- less than 18
- unable to read or understand consent form
- unable to swallow capsules
- allergy to doxycycline

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02388477
United States, Pennsylvania | |
Penn State Milton S. Hershey Medical Center | |
Hershey, Pennsylvania, United States, 17033 |
Principal Investigator: | Aman Dhawan, MD | Milton S. Hershey Medical Center |
Responsible Party: | Aman Dhawan, MD, Assistant Professor of Surgery, Orthopaedics, Milton S. Hershey Medical Center |
ClinicalTrials.gov Identifier: | NCT02388477 |
Other Study ID Numbers: |
STUDY00002143 |
First Posted: | March 17, 2015 Key Record Dates |
Last Update Posted: | May 9, 2016 |
Last Verified: | May 2016 |
rotator cuff repair Doxycycline |
Rotator Cuff Injuries Rupture Wounds and Injuries Shoulder Injuries Tendon Injuries Doxycycline |
Anti-Bacterial Agents Anti-Infective Agents Antimalarials Antiprotozoal Agents Antiparasitic Agents |