The Effect of Platelet Rich Pasma on Strenal Healing Post Median Strenotomy in Patients Undergoing Open Heart Surgery
NCT ID: NCT04639089
Last Updated: 2022-02-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
50 participants
INTERVENTIONAL
2020-08-14
2023-12-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Because it is an autogenous preparation, PRP is inherently safe and therefore free from concerns over transmissible diseases such as HIV and hepatitis.
Its power of regeneration already proved by orthopedics and dentists in their trials to regenerate cartilages .We will use it to know its ability to enhance healing of sternum in vulnerable patients to sternal dehiscence after open heart surgery .
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Autologous Platelet-rich Plasma (aPRP) for Complex Aortic Arch Surgerymacrovascular Operation
NCT02572440
Topical Tranexamic Acid and Acute Blood Loss in Total Knee Arthroplasty
NCT01370460
Tranexamic Acid Usage in Bilateral Mastectomy to Reduce Post-surgical Drainage
NCT05554211
Use of PRP in Open Surgery for Type A Aortic Dissection
NCT07005661
Post-Market Clinical Study to Confirm Safety and Performance of PuraStat Absorbable Haemostatic Material for the Management of Bleeding in Liver Surgery
NCT03600168
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
2. AIM/ OBJECTIVES :
To study the Effect of platlet rich plasma on sternal healing post median sternotomy in Patients undergoing open heart surgery
3. METHODOLOGY:
* Type of Study: prospective clinical trial propensity matched comparative study
* Study Setting: Patients refered to our Cardiothoracic department, Faculty of medicine, Ain Shams University and ain shams specialized hospital to perform open heart surgery who fulfill our inclusion charateria.
* Study Period: It will be performed between march 2020 and january2022
* Study Population:
\- Inclusion Criteria: Patients with one of which
1. patients will under go open heart surgery with BMI \>30 or
2. diabetic patients
3. patients with history of chest wall radiotherapy exposure or
4. bilateral internal mammary artery harvesting .
5. age \> 70 years old -Exclusion Criteria:
<!-- -->
1. patient with history of open heart surgery
2. patients with preoperative HB level \<11
3. All emergency and urgency cardiothoracic surgery
* Sampling Method: prospective clinical trials propensity matched comparative study.
* Sample Size: 50 patients
* Ethical Considerations: All the patients will sign an informed consent for operation and for being involved in the research and follow up process .
* Study Tools: platlets rich plasma
* Preparation technique : ultra centrifuge technique
* Study Procedures:
Patient data will be collected preoperatively and intraoperatively and these risk factors will be studied Patients will be distributed to two equal groups. Demographic data : Age - gender - weight - BMI-DM-hist. of radiotherapy exposure -BIMA
Intraoperative :
We will apply 10cm plasma contain 1 million platlets on the sternal edge of only one group of them before sternal closure.
post-operative The patients will be followed till being discharged from hospital and after the first 3 months after surgery sternal stability and absence of dehiscence will be primary out come measure
Secondary end point :
Severe form of sternal deheiscence After 3months: stability of sternum will be assessed By CT chest with 3D bone reconstruction and the value of bone density as aconfirmatory test
* Statistical Analysis:using the arithmetic mean, standard deviation using hypothesis student's "t" tests for quantitative data analysis, while qualitative data (ordinal, categorical) will be analyzed using The chi-square test (x2) (Fisher's Exact Test). For all statistical comparisons, a P value of \<0.05 will be considered significant and a P value of \<0.01 will be considered highly significant.
* Statistical Package:Data will be statistically analyzed using statistical package of social science (SPSS)
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
Intraoperative :
We will apply 10cm plasma contain 1 million platlets on the sternal edge of only one group of them before sternal closure.
post-operative The patients will be followed till being discharged from hospital and after the first 3 months after surgery sternal stability and absence of dehiscence will be primary out come measure
Secondary end point :
Severe form of sternal deheiscence After 3months: stability of sternum will be assessed By CT chest with 3D bone reconstruction and the value of bone density as aconfirmatory test
PREVENTION
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
We will apply 10cm plasma contain 1 million platlets on the sternal edge before sternal closure
We will apply 10cm plasma contain 1 million platlets on the sternal edge before sternal closure
platlet rich plasma on sternal healing post median sternotomy
Patient data will be collected preoperatively and intraoperatively and these risk factors will be studied Patients will be distributed to two equal groups. Demographic data : Age - gender - weight - BMI-DM-hist. of radiotherapy exposure -BIMA
Intraoperative :
We will apply 10cm plasma contain 1 million platlets on the sternal edge of only one group of them before sternal closure.
post-operative The patients will be followed till being discharged from hospital and after the first 3 months after surgery
We will apply 10cm saline on the sternal edge before sternal closure
We will apply 10cm saline on the sternal edge before sternal closure
platlet rich plasma on sternal healing post median sternotomy
Patient data will be collected preoperatively and intraoperatively and these risk factors will be studied Patients will be distributed to two equal groups. Demographic data : Age - gender - weight - BMI-DM-hist. of radiotherapy exposure -BIMA
Intraoperative :
We will apply 10cm plasma contain 1 million platlets on the sternal edge of only one group of them before sternal closure.
post-operative The patients will be followed till being discharged from hospital and after the first 3 months after surgery
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
platlet rich plasma on sternal healing post median sternotomy
Patient data will be collected preoperatively and intraoperatively and these risk factors will be studied Patients will be distributed to two equal groups. Demographic data : Age - gender - weight - BMI-DM-hist. of radiotherapy exposure -BIMA
Intraoperative :
We will apply 10cm plasma contain 1 million platlets on the sternal edge of only one group of them before sternal closure.
post-operative The patients will be followed till being discharged from hospital and after the first 3 months after surgery
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
1. patients will under go open heart surgery with BMI \>30 or
2. diabetic patients
3. patients with history of chest wall radiotherapy exposure or
4. bilateral internal mammary artery harvesting .
5. age \> 70 years old
Exclusion Criteria
70 Years
90 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Dr. Hamdy Singab
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dr. Hamdy Singab
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
hamdy singab, PHD
Role: STUDY_DIRECTOR
faculty of medicine,ain shams unversity
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hamdy Singab
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
References
Explore related publications, articles, or registry entries linked to this study.
Carlson NE, Roach RB Jr. Platelet-rich plasma: clinical applications in dentistry. J Am Dent Assoc. 2002 Oct;133(10):1383-6. doi: 10.14219/jada.archive.2002.0054.
Dhurat R, Sukesh M. Principles and Methods of Preparation of Platelet-Rich Plasma: A Review and Author's Perspective. J Cutan Aesthet Surg. 2014 Oct-Dec;7(4):189-97. doi: 10.4103/0974-2077.150734.
Kassolis JD, Rosen PS, Reynolds MA. Alveolar ridge and sinus augmentation utilizing platelet-rich plasma in combination with freeze-dried bone allograft: case series. J Periodontol. 2000 Oct;71(10):1654-61. doi: 10.1902/jop.2000.71.10.1654.
Liu Y, Kalen A, Risto O, Wahlstrom O. Fibroblast proliferation due to exposure to a platelet concentrate in vitro is pH dependent. Wound Repair Regen. 2002 Sep-Oct;10(5):336-40. doi: 10.1046/j.1524-475x.2002.10510.x.
Marx RE, Carlson ER, Eichstaedt RM, Schimmele SR, Strauss JE, Georgeff KR. Platelet-rich plasma: Growth factor enhancement for bone grafts. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1998 Jun;85(6):638-46. doi: 10.1016/s1079-2104(98)90029-4.
Dawood AS, Salem HA. Current clinical applications of platelet-rich plasma in various gynecological disorders: An appraisal of theory and practice. Clin Exp Reprod Med. 2018 Jun;45(2):67-74. doi: 10.5653/cerm.2018.45.2.67. Epub 2018 Jun 29.
Everts PA, Knape JT, Weibrich G, Schonberger JP, Hoffmann J, Overdevest EP, Box HA, van Zundert A. Platelet-rich plasma and platelet gel: a review. J Extra Corpor Technol. 2006 Jun;38(2):174-87.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
MD166/2020
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.