Skip to content

Prospective Study of Video-assisted Rib Planting in Chest Wall Stabilization

Prospective Study of Video-assisted Rib Planting in Chest Wall Stabilization

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05340517
Enrollment
20
Registered
2022-04-22
Start date
2021-02-22
Completion date
2022-01-06
Last updated
2022-04-22

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

Conditions

Rib Fracture Multiple, Rib Fractures

Keywords

internal fixation, video-assisted, chest wall stabilization, prospective study

Brief summary

The purpose of this study is to compare the advantages and disadvantages of video-assisted rib planting and traditional internal fixation of rib fractures in chest wall stabilization. The investigators design a new surgical method of video-assisted thoracoscopic surgery for rib fractures, evaluate the advantages and disadvantages of the new surgical techniques with a prospective study.

Interventions

PROCEDUREvideo-assisted rib planting

Give the patient intercostal nerve block and laryngeal mask anesthesia, after that, put the patient in lateral position. Make a 4-6cm posterolateral incision along the lower edge of the scapula,sever latissimus dorsi and serratus anterior and reach the rib surface. Lift the scapula with the abdominal retractor (or xiphoid retractor), Free adhesion tissue inside the scapula and put in the thoracoscopic lens. Free the tissue of the upper and lower edges of the ribs carefully, reset ribs and insert rib plate, which is fixed by 90° electric drill and locking screw.

Sponsors

Weigang Zhao
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

-≥3 unilateral rib displacement fractures * 18-70 years old * ASA score I-II * Preoperative arterial oxygen partial pressure \>60mmHg * Carbon dioxide partial pressure \<50mmHg

Exclusion criteria

* The distance from the broken end of the posterior rib fracture to the spine is less than 2cm * Airway stenosis * Abnormal coagulation system * History of peptic ulcer or bleeding * History of allergy to anesthesia related drugs * History of asthma or chronic obstructive pulmonary emphysema * Pregnant women

Design outcomes

Primary

MeasureTime frameDescription
The pain score after operation6 hours after operationThe investigators evaluate and record the patients' pain score after operation by visual analog scale (VAS),which is used to evaluate pain scores 6h,12h,and 24h after the operation. 0-10 is used to represent different degrees of pain, 0 is painless and 10 is severe pain. The grading criteria of pain were: 0: no pain; 1-3: mild pain; 4-6: moderate pain; 7-10: severe pain.

Secondary

MeasureTime frameDescription
The postoperative drainage7 days at mostThe investigators record the postoperative drainage of patients.The drainage of chest catheter or negative pressure ball was recorded by the nurse every day after surgery. Less postoperative drainage means faster recovery and shorter discharge times.

Other

MeasureTime frameDescription
The length of incisionDuring surgeryThe investigators record the length of operative incision.
The intraoperative bleedingDuring surgeryThe investigators record the intraoperative bleeding of patients.
The treatment costsfrom the date of hospitalization to the date of leave hospital,assessed up to 100 monthsThe investigators record the treatment costs and calculate per capita treatment costs of patients,which is recorded and counted at the time of discharge. Total treatment costs include hospitalization, treatment, surgery, medications, and other related expenses.
The operation timeDuring surgeryThe investigators record patients' operation time duration.
Days of stay hospitalfrom the date of hospitalization to the date of leave hospital,assessed up to 100 monthsDays of stay hospital

Countries

China

Outcome results

None listed

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